Target Gene/Pathway Pathway / Gene

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No.	KEGG PATHWAY On map, Yellow: Drug target, Red: All disease-related	KEGG GENES	KEGG DRUG	DrugBank	Disease ID
1	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
2	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
3	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
4	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
5	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 5. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
6	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 5. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
7	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 7. Adrenergic signaling in cardiomyocytes × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
8	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 8. Adrenergic signaling in cardiomyocytes × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
9	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 9. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
10	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 9. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
11	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 9. Adrenergic signaling in cardiomyocytes × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
12	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 12. Adrenergic signaling in cardiomyocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 13. Adrenergic signaling in cardiomyocytes × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
14	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 13. Adrenergic signaling in cardiomyocytes × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
15	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 15. Adrenergic signaling in cardiomyocytes × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
16	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 16. Adrenergic signaling in cardiomyocytes × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
17	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 17. Adrenergic signaling in cardiomyocytes × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
18	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 17. Adrenergic signaling in cardiomyocytes × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
19	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 19. Adrenergic signaling in cardiomyocytes × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
20	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 19. Adrenergic signaling in cardiomyocytes × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
21	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 21. Adrenergic signaling in cardiomyocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
22	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 22. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
23	Adrenergic signaling in cardiomyocytes 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 22. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
24	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Aldosterone synthesis and secretion × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 24. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
25	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Aldosterone synthesis and secretion × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 24. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
26	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Aldosterone synthesis and secretion × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 24. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
27	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Aldosterone synthesis and secretion × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 24. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
28	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 28. Aldosterone synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
29	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Aldosterone synthesis and secretion × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 28. Aldosterone synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
30	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 30. Aldosterone synthesis and secretion × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
31	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Aldosterone synthesis and secretion × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 31. Aldosterone synthesis and secretion × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
32	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 32. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
33	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Aldosterone synthesis and secretion × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 32. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
34	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Aldosterone synthesis and secretion × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 32. Aldosterone synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
35	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Aldosterone synthesis and secretion × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 35. Aldosterone synthesis and secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
36	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 36. Aldosterone synthesis and secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
37	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Aldosterone synthesis and secretion × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 36. Aldosterone synthesis and secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
38	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Aldosterone synthesis and secretion × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 38. Aldosterone synthesis and secretion × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
39	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Aldosterone synthesis and secretion × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 39. Aldosterone synthesis and secretion × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
40	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Aldosterone synthesis and secretion × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 40. Aldosterone synthesis and secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
41	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Aldosterone synthesis and secretion × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 40. Aldosterone synthesis and secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
42	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 42. Aldosterone synthesis and secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
43	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Aldosterone synthesis and secretion × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 42. Aldosterone synthesis and secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
44	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Aldosterone synthesis and secretion × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 44. Aldosterone synthesis and secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
45	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Aldosterone synthesis and secretion × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 45. Aldosterone synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
46	Aldosterone synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Aldosterone synthesis and secretion × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 45. Aldosterone synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
47	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Alzheimer disease × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 47. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
48	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Alzheimer disease × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 47. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
49	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Alzheimer disease × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 47. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
50	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Alzheimer disease × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 47. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
51	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Alzheimer disease × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 51. Alzheimer disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
52	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Alzheimer disease × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 51. Alzheimer disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
53	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Alzheimer disease × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 53. Alzheimer disease × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
54	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Alzheimer disease × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 54. Alzheimer disease × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
55	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Alzheimer disease × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 55. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
56	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Alzheimer disease × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 55. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
57	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Alzheimer disease × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 55. Alzheimer disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
58	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Alzheimer disease × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 58. Alzheimer disease × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
59	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Alzheimer disease × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 59. Alzheimer disease × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
60	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Alzheimer disease × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 59. Alzheimer disease × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
61	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Alzheimer disease × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 61. Alzheimer disease × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
62	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Alzheimer disease × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 62. Alzheimer disease × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
63	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Alzheimer disease × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 63. Alzheimer disease × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
64	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Alzheimer disease × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 63. Alzheimer disease × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
65	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Alzheimer disease × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 65. Alzheimer disease × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
66	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Alzheimer disease × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 65. Alzheimer disease × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
67	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Alzheimer disease × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 67. Alzheimer disease × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
68	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Alzheimer disease × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 68. Alzheimer disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
69	Alzheimer disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Alzheimer disease × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 68. Alzheimer disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
70	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Amphetamine addiction × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 70. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
71	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Amphetamine addiction × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 70. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
72	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Amphetamine addiction × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 70. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
73	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Amphetamine addiction × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 70. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
74	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Amphetamine addiction × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 74. Amphetamine addiction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
75	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Amphetamine addiction × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 74. Amphetamine addiction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
76	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Amphetamine addiction × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 76. Amphetamine addiction × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
77	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Amphetamine addiction × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 77. Amphetamine addiction × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
78	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Amphetamine addiction × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 78. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
79	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Amphetamine addiction × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 78. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
80	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Amphetamine addiction × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 78. Amphetamine addiction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
81	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Amphetamine addiction × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 81. Amphetamine addiction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
82	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Amphetamine addiction × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 82. Amphetamine addiction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
83	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Amphetamine addiction × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 82. Amphetamine addiction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
84	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Amphetamine addiction × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 84. Amphetamine addiction × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
85	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Amphetamine addiction × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 85. Amphetamine addiction × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
86	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Amphetamine addiction × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 86. Amphetamine addiction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
87	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Amphetamine addiction × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 86. Amphetamine addiction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
88	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Amphetamine addiction × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 88. Amphetamine addiction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
89	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Amphetamine addiction × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 88. Amphetamine addiction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
90	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Amphetamine addiction × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 90. Amphetamine addiction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
91	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Amphetamine addiction × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 91. Amphetamine addiction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
92	Amphetamine addiction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Amphetamine addiction × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 91. Amphetamine addiction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
93	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 93. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
94	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 93. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
95	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 93. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
96	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 93. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
97	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 97. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
98	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 97. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
99	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 99. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
100	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 100. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
101	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 101. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
102	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 101. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
103	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 101. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
104	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 104. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
105	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 105. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
106	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 105. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
107	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 107. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
108	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 108. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
109	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 109. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
110	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 109. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
111	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 111. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
112	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 111. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
113	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 113. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
114	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 114. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
115	Arrhythmogenic right ventricular cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Arrhythmogenic right ventricular cardiomyopathy × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 114. Arrhythmogenic right ventricular cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
116	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Calcium signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 116. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
117	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Calcium signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 116. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
118	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Calcium signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 116. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
119	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Calcium signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 116. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
120	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Calcium signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 120. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
121	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Calcium signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 120. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
122	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Calcium signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 122. Calcium signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
123	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Calcium signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 123. Calcium signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
124	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Calcium signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 124. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
125	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Calcium signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 124. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
126	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Calcium signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 124. Calcium signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
127	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Calcium signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 127. Calcium signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
128	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Calcium signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 128. Calcium signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
129	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Calcium signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 128. Calcium signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
130	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Calcium signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 130. Calcium signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
131	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Calcium signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 131. Calcium signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
132	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Calcium signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 132. Calcium signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
133	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Calcium signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 132. Calcium signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
134	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Calcium signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 134. Calcium signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
135	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Calcium signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 134. Calcium signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
136	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Calcium signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 136. Calcium signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
137	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Calcium signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 137. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
138	Calcium signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Calcium signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 137. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
139	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 cAMP signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 139. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
140	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 cAMP signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 139. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
141	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 cAMP signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 139. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
142	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 cAMP signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 139. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
143	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 cAMP signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 143. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
144	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 cAMP signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 143. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
145	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 cAMP signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 145. cAMP signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
146	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 cAMP signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 146. cAMP signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
147	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 cAMP signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 147. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
148	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 cAMP signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 147. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
149	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 cAMP signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 147. cAMP signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
150	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 cAMP signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 150. cAMP signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
151	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 cAMP signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 151. cAMP signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
152	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 cAMP signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 151. cAMP signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
153	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 cAMP signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 153. cAMP signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
154	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 cAMP signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 154. cAMP signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
155	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 cAMP signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 155. cAMP signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
156	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 cAMP signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 155. cAMP signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
157	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 cAMP signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 157. cAMP signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
158	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 cAMP signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 157. cAMP signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
159	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 cAMP signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 159. cAMP signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
160	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 cAMP signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 160. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
161	cAMP signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 cAMP signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 160. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
162	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Carbohydrate digestion and absorption × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 162. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
163	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Carbohydrate digestion and absorption × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 162. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
164	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Carbohydrate digestion and absorption × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 162. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
165	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Carbohydrate digestion and absorption × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 162. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
166	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 166. Carbohydrate digestion and absorption × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
167	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Carbohydrate digestion and absorption × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 166. Carbohydrate digestion and absorption × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
168	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 168. Carbohydrate digestion and absorption × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
169	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Carbohydrate digestion and absorption × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 169. Carbohydrate digestion and absorption × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
170	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 170. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
171	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Carbohydrate digestion and absorption × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 170. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
172	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Carbohydrate digestion and absorption × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 170. Carbohydrate digestion and absorption × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
173	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Carbohydrate digestion and absorption × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 173. Carbohydrate digestion and absorption × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
174	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 174. Carbohydrate digestion and absorption × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
175	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Carbohydrate digestion and absorption × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 174. Carbohydrate digestion and absorption × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
176	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Carbohydrate digestion and absorption × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 176. Carbohydrate digestion and absorption × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
177	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Carbohydrate digestion and absorption × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 177. Carbohydrate digestion and absorption × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
178	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Carbohydrate digestion and absorption × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 178. Carbohydrate digestion and absorption × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
179	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Carbohydrate digestion and absorption × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 178. Carbohydrate digestion and absorption × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
180	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 180. Carbohydrate digestion and absorption × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
181	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Carbohydrate digestion and absorption × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 180. Carbohydrate digestion and absorption × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
182	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Carbohydrate digestion and absorption × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 182. Carbohydrate digestion and absorption × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
183	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Carbohydrate digestion and absorption × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 183. Carbohydrate digestion and absorption × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
184	Carbohydrate digestion and absorption 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Carbohydrate digestion and absorption × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 183. Carbohydrate digestion and absorption × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
185	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Cardiac muscle contraction × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 185. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
186	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Cardiac muscle contraction × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 185. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
187	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Cardiac muscle contraction × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 185. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
188	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Cardiac muscle contraction × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 185. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
189	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Cardiac muscle contraction × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 189. Cardiac muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
190	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Cardiac muscle contraction × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 189. Cardiac muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
191	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Cardiac muscle contraction × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 191. Cardiac muscle contraction × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
192	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Cardiac muscle contraction × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 192. Cardiac muscle contraction × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
193	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Cardiac muscle contraction × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 193. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
194	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Cardiac muscle contraction × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 193. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
195	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Cardiac muscle contraction × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 193. Cardiac muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
196	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Cardiac muscle contraction × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 196. Cardiac muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
197	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Cardiac muscle contraction × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 197. Cardiac muscle contraction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
198	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Cardiac muscle contraction × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 197. Cardiac muscle contraction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
199	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Cardiac muscle contraction × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 199. Cardiac muscle contraction × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
200	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Cardiac muscle contraction × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 200. Cardiac muscle contraction × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
201	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Cardiac muscle contraction × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 201. Cardiac muscle contraction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
202	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Cardiac muscle contraction × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 201. Cardiac muscle contraction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
203	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Cardiac muscle contraction × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 203. Cardiac muscle contraction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
204	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Cardiac muscle contraction × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 203. Cardiac muscle contraction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
205	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Cardiac muscle contraction × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 205. Cardiac muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
206	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Cardiac muscle contraction × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 206. Cardiac muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
207	Cardiac muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Cardiac muscle contraction × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 206. Cardiac muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
208	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Cellular senescence × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 208. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
209	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Cellular senescence × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 208. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
210	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Cellular senescence × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 208. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
211	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Cellular senescence × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 208. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
212	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Cellular senescence × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 212. Cellular senescence × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
213	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Cellular senescence × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 212. Cellular senescence × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
214	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Cellular senescence × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 214. Cellular senescence × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
215	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Cellular senescence × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 215. Cellular senescence × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
216	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Cellular senescence × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 216. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
217	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Cellular senescence × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 216. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
218	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Cellular senescence × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 216. Cellular senescence × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
219	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Cellular senescence × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 219. Cellular senescence × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
220	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Cellular senescence × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 220. Cellular senescence × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
221	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Cellular senescence × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 220. Cellular senescence × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
222	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Cellular senescence × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 222. Cellular senescence × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
223	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Cellular senescence × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 223. Cellular senescence × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
224	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Cellular senescence × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 224. Cellular senescence × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
225	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Cellular senescence × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 224. Cellular senescence × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
226	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Cellular senescence × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 226. Cellular senescence × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
227	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Cellular senescence × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 226. Cellular senescence × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
228	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Cellular senescence × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 228. Cellular senescence × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
229	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Cellular senescence × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 229. Cellular senescence × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
230	Cellular senescence 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Cellular senescence × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 229. Cellular senescence × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
231	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 cGMP-PKG signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 231. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
232	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 cGMP-PKG signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 231. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
233	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 cGMP-PKG signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 231. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
234	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 cGMP-PKG signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 231. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
235	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 235. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
236	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 cGMP-PKG signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 235. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
237	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 237. cGMP-PKG signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
238	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 cGMP-PKG signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 238. cGMP-PKG signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
239	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 239. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
240	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 cGMP-PKG signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 239. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
241	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 cGMP-PKG signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 239. cGMP-PKG signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
242	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 cGMP-PKG signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 242. cGMP-PKG signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
243	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 243. cGMP-PKG signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
244	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 cGMP-PKG signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 243. cGMP-PKG signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
245	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 cGMP-PKG signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 245. cGMP-PKG signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
246	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 cGMP-PKG signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 246. cGMP-PKG signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
247	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 cGMP-PKG signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 247. cGMP-PKG signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
248	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 cGMP-PKG signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 247. cGMP-PKG signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
249	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 249. cGMP-PKG signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
250	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 cGMP-PKG signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 249. cGMP-PKG signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
251	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 cGMP-PKG signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 251. cGMP-PKG signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
252	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 252. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
253	cGMP-PKG signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 cGMP-PKG signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 252. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
254	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 254. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
255	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 254. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
256	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 254. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
257	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 254. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
258	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 258. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
259	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 258. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
260	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 260. Chemical carcinogenesis - receptor activation × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
261	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 261. Chemical carcinogenesis - receptor activation × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
262	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 262. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
263	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 262. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
264	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Chemical carcinogenesis - receptor activation × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 262. Chemical carcinogenesis - receptor activation × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
265	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 265. Chemical carcinogenesis - receptor activation × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
266	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 266. Chemical carcinogenesis - receptor activation × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
267	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 266. Chemical carcinogenesis - receptor activation × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
268	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 268. Chemical carcinogenesis - receptor activation × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
269	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 269. Chemical carcinogenesis - receptor activation × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
270	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 270. Chemical carcinogenesis - receptor activation × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
271	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Chemical carcinogenesis - receptor activation × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 270. Chemical carcinogenesis - receptor activation × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
272	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 272. Chemical carcinogenesis - receptor activation × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
273	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 272. Chemical carcinogenesis - receptor activation × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
274	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 274. Chemical carcinogenesis - receptor activation × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
275	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 275. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
276	Chemical carcinogenesis - receptor activation 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Chemical carcinogenesis - receptor activation × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 275. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
277	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Cholinergic synapse × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 277. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
278	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Cholinergic synapse × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 277. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
279	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Cholinergic synapse × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 277. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
280	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Cholinergic synapse × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 277. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
281	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Cholinergic synapse × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 281. Cholinergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
282	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Cholinergic synapse × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 281. Cholinergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
283	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Cholinergic synapse × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 283. Cholinergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
284	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Cholinergic synapse × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 284. Cholinergic synapse × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
285	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Cholinergic synapse × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 285. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
286	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Cholinergic synapse × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 285. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
287	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Cholinergic synapse × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 285. Cholinergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
288	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Cholinergic synapse × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 288. Cholinergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
289	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Cholinergic synapse × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 289. Cholinergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
290	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Cholinergic synapse × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 289. Cholinergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
291	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Cholinergic synapse × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 291. Cholinergic synapse × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
292	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Cholinergic synapse × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 292. Cholinergic synapse × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
293	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Cholinergic synapse × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 293. Cholinergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
294	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Cholinergic synapse × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 293. Cholinergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
295	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Cholinergic synapse × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 295. Cholinergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
296	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Cholinergic synapse × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 295. Cholinergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
297	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Cholinergic synapse × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 297. Cholinergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
298	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Cholinergic synapse × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 298. Cholinergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
299	Cholinergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Cholinergic synapse × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 298. Cholinergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
300	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Circadian entrainment × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 300. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
301	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Circadian entrainment × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 300. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
302	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Circadian entrainment × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 300. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
303	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Circadian entrainment × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 300. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
304	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Circadian entrainment × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 304. Circadian entrainment × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
305	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Circadian entrainment × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 304. Circadian entrainment × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
306	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Circadian entrainment × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 306. Circadian entrainment × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
307	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Circadian entrainment × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 307. Circadian entrainment × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
308	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Circadian entrainment × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 308. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
309	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Circadian entrainment × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 308. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
310	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Circadian entrainment × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 308. Circadian entrainment × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
311	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Circadian entrainment × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 311. Circadian entrainment × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
312	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Circadian entrainment × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 312. Circadian entrainment × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
313	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Circadian entrainment × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 312. Circadian entrainment × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
314	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Circadian entrainment × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 314. Circadian entrainment × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
315	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Circadian entrainment × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 315. Circadian entrainment × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
316	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Circadian entrainment × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 316. Circadian entrainment × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
317	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Circadian entrainment × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 316. Circadian entrainment × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
318	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Circadian entrainment × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 318. Circadian entrainment × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
319	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Circadian entrainment × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 318. Circadian entrainment × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
320	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Circadian entrainment × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 320. Circadian entrainment × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
321	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Circadian entrainment × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 321. Circadian entrainment × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
322	Circadian entrainment 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Circadian entrainment × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 321. Circadian entrainment × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
323	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Cortisol synthesis and secretion × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 323. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
324	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Cortisol synthesis and secretion × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 323. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
325	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Cortisol synthesis and secretion × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 323. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
326	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Cortisol synthesis and secretion × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 323. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
327	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 327. Cortisol synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
328	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Cortisol synthesis and secretion × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 327. Cortisol synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
329	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 329. Cortisol synthesis and secretion × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
330	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Cortisol synthesis and secretion × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 330. Cortisol synthesis and secretion × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
331	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 331. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
332	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Cortisol synthesis and secretion × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 331. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
333	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Cortisol synthesis and secretion × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 331. Cortisol synthesis and secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
334	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Cortisol synthesis and secretion × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 334. Cortisol synthesis and secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
335	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 335. Cortisol synthesis and secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
336	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Cortisol synthesis and secretion × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 335. Cortisol synthesis and secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
337	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Cortisol synthesis and secretion × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 337. Cortisol synthesis and secretion × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
338	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Cortisol synthesis and secretion × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 338. Cortisol synthesis and secretion × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
339	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Cortisol synthesis and secretion × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 339. Cortisol synthesis and secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
340	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Cortisol synthesis and secretion × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 339. Cortisol synthesis and secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
341	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 341. Cortisol synthesis and secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
342	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Cortisol synthesis and secretion × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 341. Cortisol synthesis and secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
343	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Cortisol synthesis and secretion × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 343. Cortisol synthesis and secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
344	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Cortisol synthesis and secretion × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 344. Cortisol synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
345	Cortisol synthesis and secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Cortisol synthesis and secretion × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 344. Cortisol synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
346	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Cushing syndrome × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 346. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
347	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Cushing syndrome × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 346. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
348	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Cushing syndrome × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 346. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
349	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Cushing syndrome × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 346. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
350	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Cushing syndrome × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 350. Cushing syndrome × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
351	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Cushing syndrome × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 350. Cushing syndrome × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
352	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Cushing syndrome × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 352. Cushing syndrome × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
353	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Cushing syndrome × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 353. Cushing syndrome × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
354	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Cushing syndrome × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 354. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
355	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Cushing syndrome × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 354. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
356	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Cushing syndrome × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 354. Cushing syndrome × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
357	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Cushing syndrome × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 357. Cushing syndrome × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
358	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Cushing syndrome × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 358. Cushing syndrome × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
359	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Cushing syndrome × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 358. Cushing syndrome × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
360	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Cushing syndrome × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 360. Cushing syndrome × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
361	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Cushing syndrome × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 361. Cushing syndrome × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
362	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Cushing syndrome × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 362. Cushing syndrome × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
363	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Cushing syndrome × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 362. Cushing syndrome × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
364	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Cushing syndrome × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 364. Cushing syndrome × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
365	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Cushing syndrome × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 364. Cushing syndrome × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
366	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Cushing syndrome × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 366. Cushing syndrome × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
367	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Cushing syndrome × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 367. Cushing syndrome × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
368	Cushing syndrome 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Cushing syndrome × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 367. Cushing syndrome × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
369	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Dilated cardiomyopathy × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 369. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
370	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Dilated cardiomyopathy × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 369. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
371	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Dilated cardiomyopathy × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 369. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
372	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Dilated cardiomyopathy × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 369. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
373	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 373. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
374	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Dilated cardiomyopathy × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 373. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
375	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 375. Dilated cardiomyopathy × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
376	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Dilated cardiomyopathy × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 376. Dilated cardiomyopathy × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
377	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 377. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
378	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Dilated cardiomyopathy × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 377. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
379	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Dilated cardiomyopathy × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 377. Dilated cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
380	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Dilated cardiomyopathy × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 380. Dilated cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
381	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 381. Dilated cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
382	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Dilated cardiomyopathy × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 381. Dilated cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
383	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Dilated cardiomyopathy × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 383. Dilated cardiomyopathy × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
384	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Dilated cardiomyopathy × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 384. Dilated cardiomyopathy × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
385	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Dilated cardiomyopathy × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 385. Dilated cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
386	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Dilated cardiomyopathy × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 385. Dilated cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
387	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 387. Dilated cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
388	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Dilated cardiomyopathy × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 387. Dilated cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
389	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Dilated cardiomyopathy × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 389. Dilated cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
390	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 390. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
391	Dilated cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Dilated cardiomyopathy × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 390. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
392	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Dopaminergic synapse × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 392. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
393	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Dopaminergic synapse × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 392. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
394	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Dopaminergic synapse × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 392. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
395	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Dopaminergic synapse × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 392. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
396	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Dopaminergic synapse × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 396. Dopaminergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
397	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Dopaminergic synapse × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 396. Dopaminergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
398	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Dopaminergic synapse × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 398. Dopaminergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
399	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Dopaminergic synapse × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 399. Dopaminergic synapse × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
400	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Dopaminergic synapse × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 400. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
401	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Dopaminergic synapse × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 400. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
402	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Dopaminergic synapse × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 400. Dopaminergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
403	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Dopaminergic synapse × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 403. Dopaminergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
404	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Dopaminergic synapse × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 404. Dopaminergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
405	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Dopaminergic synapse × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 404. Dopaminergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
406	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Dopaminergic synapse × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 406. Dopaminergic synapse × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
407	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Dopaminergic synapse × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 407. Dopaminergic synapse × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
408	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Dopaminergic synapse × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 408. Dopaminergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
409	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Dopaminergic synapse × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 408. Dopaminergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
410	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Dopaminergic synapse × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 410. Dopaminergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
411	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Dopaminergic synapse × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 410. Dopaminergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
412	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Dopaminergic synapse × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 412. Dopaminergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
413	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Dopaminergic synapse × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 413. Dopaminergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
414	Dopaminergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Dopaminergic synapse × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 413. Dopaminergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
415	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 GABAergic synapse × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 415. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
416	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 GABAergic synapse × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 415. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
417	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 GABAergic synapse × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 415. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
418	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 GABAergic synapse × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 415. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
419	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 GABAergic synapse × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 419. GABAergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
420	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 GABAergic synapse × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 419. GABAergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
421	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 GABAergic synapse × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 421. GABAergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
422	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 GABAergic synapse × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 422. GABAergic synapse × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
423	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 GABAergic synapse × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 423. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
424	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 GABAergic synapse × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 423. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
425	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 GABAergic synapse × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 423. GABAergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
426	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 GABAergic synapse × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 426. GABAergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
427	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 GABAergic synapse × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 427. GABAergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
428	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 GABAergic synapse × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 427. GABAergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
429	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 GABAergic synapse × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 429. GABAergic synapse × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
430	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 GABAergic synapse × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 430. GABAergic synapse × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
431	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 GABAergic synapse × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 431. GABAergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
432	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 GABAergic synapse × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 431. GABAergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
433	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 GABAergic synapse × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 433. GABAergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
434	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 GABAergic synapse × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 433. GABAergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
435	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 GABAergic synapse × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 435. GABAergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
436	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 GABAergic synapse × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 436. GABAergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
437	GABAergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 GABAergic synapse × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 436. GABAergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
438	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Glutamatergic synapse × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 438. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
439	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Glutamatergic synapse × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 438. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
440	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Glutamatergic synapse × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 438. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
441	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Glutamatergic synapse × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 438. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
442	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Glutamatergic synapse × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 442. Glutamatergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
443	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Glutamatergic synapse × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 442. Glutamatergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
444	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Glutamatergic synapse × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 444. Glutamatergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
445	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Glutamatergic synapse × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 445. Glutamatergic synapse × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
446	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Glutamatergic synapse × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 446. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
447	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Glutamatergic synapse × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 446. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
448	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Glutamatergic synapse × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 446. Glutamatergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
449	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Glutamatergic synapse × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 449. Glutamatergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
450	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Glutamatergic synapse × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 450. Glutamatergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
451	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Glutamatergic synapse × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 450. Glutamatergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
452	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Glutamatergic synapse × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 452. Glutamatergic synapse × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
453	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Glutamatergic synapse × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 453. Glutamatergic synapse × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
454	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Glutamatergic synapse × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 454. Glutamatergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
455	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Glutamatergic synapse × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 454. Glutamatergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
456	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Glutamatergic synapse × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 456. Glutamatergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
457	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Glutamatergic synapse × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 456. Glutamatergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
458	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Glutamatergic synapse × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 458. Glutamatergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
459	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Glutamatergic synapse × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 459. Glutamatergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
460	Glutamatergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Glutamatergic synapse × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 459. Glutamatergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
461	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 GnRH secretion × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 461. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
462	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 GnRH secretion × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 461. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
463	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 GnRH secretion × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 461. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
464	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 GnRH secretion × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 461. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
465	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 GnRH secretion × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 465. GnRH secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
466	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 GnRH secretion × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 465. GnRH secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
467	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 GnRH secretion × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 467. GnRH secretion × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
468	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 GnRH secretion × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 468. GnRH secretion × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
469	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 GnRH secretion × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 469. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
470	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 GnRH secretion × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 469. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
471	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 GnRH secretion × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 469. GnRH secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
472	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 GnRH secretion × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 472. GnRH secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
473	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 GnRH secretion × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 473. GnRH secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
474	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 GnRH secretion × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 473. GnRH secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
475	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 GnRH secretion × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 475. GnRH secretion × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
476	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 GnRH secretion × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 476. GnRH secretion × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
477	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 GnRH secretion × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 477. GnRH secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
478	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 GnRH secretion × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 477. GnRH secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
479	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 GnRH secretion × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 479. GnRH secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
480	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 GnRH secretion × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 479. GnRH secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
481	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 GnRH secretion × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 481. GnRH secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
482	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 GnRH secretion × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 482. GnRH secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
483	GnRH secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 GnRH secretion × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 482. GnRH secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
484	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 GnRH signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 484. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
485	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 GnRH signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 484. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
486	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 GnRH signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 484. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
487	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 GnRH signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 484. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
488	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 GnRH signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 488. GnRH signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
489	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 GnRH signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 488. GnRH signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
490	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 GnRH signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 490. GnRH signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
491	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 GnRH signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 491. GnRH signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
492	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 GnRH signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 492. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
493	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 GnRH signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 492. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
494	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 GnRH signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 492. GnRH signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
495	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 GnRH signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 495. GnRH signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
496	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 GnRH signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 496. GnRH signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
497	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 GnRH signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 496. GnRH signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
498	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 GnRH signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 498. GnRH signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
499	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 GnRH signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 499. GnRH signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
500	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 GnRH signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 500. GnRH signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
501	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 GnRH signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 500. GnRH signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
502	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 GnRH signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 502. GnRH signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
503	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 GnRH signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 502. GnRH signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
504	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 GnRH signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 504. GnRH signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
505	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 GnRH signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 505. GnRH signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
506	GnRH signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 GnRH signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 505. GnRH signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
507	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Growth hormone synthesis, secretion and action × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 507. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
508	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Growth hormone synthesis, secretion and action × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 507. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
509	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 507. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
510	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Growth hormone synthesis, secretion and action × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 507. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
511	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 511. Growth hormone synthesis, secretion and action × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
512	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 511. Growth hormone synthesis, secretion and action × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
513	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 513. Growth hormone synthesis, secretion and action × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
514	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 514. Growth hormone synthesis, secretion and action × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
515	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 515. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
516	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Growth hormone synthesis, secretion and action × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 515. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
517	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Growth hormone synthesis, secretion and action × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 515. Growth hormone synthesis, secretion and action × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
518	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 518. Growth hormone synthesis, secretion and action × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
519	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 519. Growth hormone synthesis, secretion and action × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
520	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 519. Growth hormone synthesis, secretion and action × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
521	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 521. Growth hormone synthesis, secretion and action × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
522	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Growth hormone synthesis, secretion and action × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 522. Growth hormone synthesis, secretion and action × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
523	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Growth hormone synthesis, secretion and action × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 523. Growth hormone synthesis, secretion and action × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
524	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Growth hormone synthesis, secretion and action × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 523. Growth hormone synthesis, secretion and action × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
525	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 525. Growth hormone synthesis, secretion and action × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
526	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Growth hormone synthesis, secretion and action × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 525. Growth hormone synthesis, secretion and action × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
527	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Growth hormone synthesis, secretion and action × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 527. Growth hormone synthesis, secretion and action × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
528	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Growth hormone synthesis, secretion and action × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 528. Growth hormone synthesis, secretion and action × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
529	Growth hormone synthesis, secretion and action 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Growth hormone synthesis, secretion and action × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 528. Growth hormone synthesis, secretion and action × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
530	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Hypertrophic cardiomyopathy × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 530. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
531	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Hypertrophic cardiomyopathy × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 530. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
532	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Hypertrophic cardiomyopathy × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 530. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
533	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Hypertrophic cardiomyopathy × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 530. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
534	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 534. Hypertrophic cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
535	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Hypertrophic cardiomyopathy × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 534. Hypertrophic cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
536	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 536. Hypertrophic cardiomyopathy × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
537	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Hypertrophic cardiomyopathy × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 537. Hypertrophic cardiomyopathy × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
538	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 538. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
539	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Hypertrophic cardiomyopathy × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 538. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
540	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Hypertrophic cardiomyopathy × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 538. Hypertrophic cardiomyopathy × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
541	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Hypertrophic cardiomyopathy × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 541. Hypertrophic cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
542	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 542. Hypertrophic cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
543	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Hypertrophic cardiomyopathy × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 542. Hypertrophic cardiomyopathy × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
544	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Hypertrophic cardiomyopathy × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 544. Hypertrophic cardiomyopathy × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
545	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Hypertrophic cardiomyopathy × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 545. Hypertrophic cardiomyopathy × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
546	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Hypertrophic cardiomyopathy × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 546. Hypertrophic cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
547	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Hypertrophic cardiomyopathy × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 546. Hypertrophic cardiomyopathy × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
548	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 548. Hypertrophic cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
549	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Hypertrophic cardiomyopathy × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 548. Hypertrophic cardiomyopathy × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
550	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Hypertrophic cardiomyopathy × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 550. Hypertrophic cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
551	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 551. Hypertrophic cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
552	Hypertrophic cardiomyopathy 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Hypertrophic cardiomyopathy × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 551. Hypertrophic cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
553	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Insulin secretion × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 553. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
554	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Insulin secretion × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 553. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
555	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Insulin secretion × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 553. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
556	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Insulin secretion × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 553. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
557	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Insulin secretion × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 557. Insulin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
558	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Insulin secretion × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 557. Insulin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
559	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Insulin secretion × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 559. Insulin secretion × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
560	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Insulin secretion × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 560. Insulin secretion × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
561	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Insulin secretion × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 561. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
562	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Insulin secretion × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 561. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
563	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Insulin secretion × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 561. Insulin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
564	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Insulin secretion × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 564. Insulin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
565	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Insulin secretion × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 565. Insulin secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
566	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Insulin secretion × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 565. Insulin secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
567	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Insulin secretion × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 567. Insulin secretion × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
568	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Insulin secretion × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 568. Insulin secretion × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
569	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Insulin secretion × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 569. Insulin secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
570	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Insulin secretion × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 569. Insulin secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
571	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Insulin secretion × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 571. Insulin secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
572	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Insulin secretion × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 571. Insulin secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
573	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Insulin secretion × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 573. Insulin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
574	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Insulin secretion × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 574. Insulin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
575	Insulin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Insulin secretion × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 574. Insulin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
576	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 MAPK signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 576. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
577	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 MAPK signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 576. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
578	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 MAPK signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 576. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
579	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 MAPK signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 576. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
580	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 MAPK signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 580. MAPK signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
581	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 MAPK signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 580. MAPK signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
582	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 MAPK signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 582. MAPK signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
583	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 MAPK signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 583. MAPK signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
584	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 MAPK signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 584. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
585	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 MAPK signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 584. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
586	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 MAPK signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 584. MAPK signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
587	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 MAPK signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 587. MAPK signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
588	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 MAPK signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 588. MAPK signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
589	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 MAPK signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 588. MAPK signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
590	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 MAPK signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 590. MAPK signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
591	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 MAPK signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 591. MAPK signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
592	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 MAPK signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 592. MAPK signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
593	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 MAPK signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 592. MAPK signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
594	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 MAPK signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 594. MAPK signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
595	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 MAPK signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 594. MAPK signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
596	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 MAPK signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 596. MAPK signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
597	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 MAPK signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 597. MAPK signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
598	MAPK signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 MAPK signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 597. MAPK signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
599	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Oxytocin signaling pathway × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 599. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
600	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Oxytocin signaling pathway × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 599. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
601	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Oxytocin signaling pathway × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 599. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
602	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Oxytocin signaling pathway × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 599. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
603	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 603. Oxytocin signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
604	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Oxytocin signaling pathway × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 603. Oxytocin signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
605	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 605. Oxytocin signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
606	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Oxytocin signaling pathway × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 606. Oxytocin signaling pathway × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
607	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 607. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
608	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Oxytocin signaling pathway × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 607. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
609	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Oxytocin signaling pathway × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 607. Oxytocin signaling pathway × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
610	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Oxytocin signaling pathway × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 610. Oxytocin signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
611	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 611. Oxytocin signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
612	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Oxytocin signaling pathway × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 611. Oxytocin signaling pathway × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
613	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Oxytocin signaling pathway × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 613. Oxytocin signaling pathway × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
614	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Oxytocin signaling pathway × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 614. Oxytocin signaling pathway × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
615	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Oxytocin signaling pathway × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 615. Oxytocin signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
616	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Oxytocin signaling pathway × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 615. Oxytocin signaling pathway × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
617	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 617. Oxytocin signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
618	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Oxytocin signaling pathway × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 617. Oxytocin signaling pathway × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
619	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Oxytocin signaling pathway × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 619. Oxytocin signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
620	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Oxytocin signaling pathway × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 620. Oxytocin signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
621	Oxytocin signaling pathway 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Oxytocin signaling pathway × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 620. Oxytocin signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
622	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 622. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
623	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 622. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
624	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 622. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
625	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 622. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
626	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 626. Pathways of neurodegeneration - multiple diseases × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
627	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 626. Pathways of neurodegeneration - multiple diseases × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
628	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 628. Pathways of neurodegeneration - multiple diseases × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
629	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 629. Pathways of neurodegeneration - multiple diseases × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
630	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 630. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
631	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 630. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
632	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 630. Pathways of neurodegeneration - multiple diseases × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
633	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 633. Pathways of neurodegeneration - multiple diseases × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
634	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 634. Pathways of neurodegeneration - multiple diseases × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
635	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 634. Pathways of neurodegeneration - multiple diseases × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
636	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 636. Pathways of neurodegeneration - multiple diseases × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
637	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 637. Pathways of neurodegeneration - multiple diseases × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
638	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 638. Pathways of neurodegeneration - multiple diseases × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
639	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 638. Pathways of neurodegeneration - multiple diseases × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
640	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 640. Pathways of neurodegeneration - multiple diseases × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
641	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 640. Pathways of neurodegeneration - multiple diseases × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
642	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 642. Pathways of neurodegeneration - multiple diseases × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
643	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 643. Pathways of neurodegeneration - multiple diseases × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
644	Pathways of neurodegeneration - multiple diseases 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 643. Pathways of neurodegeneration - multiple diseases × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
645	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Prion disease × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 645. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
646	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Prion disease × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 645. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
647	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Prion disease × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 645. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
648	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Prion disease × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 645. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
649	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Prion disease × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 649. Prion disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
650	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Prion disease × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 649. Prion disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
651	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Prion disease × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 651. Prion disease × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
652	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Prion disease × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 652. Prion disease × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
653	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Prion disease × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 653. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
654	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Prion disease × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 653. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
655	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Prion disease × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 653. Prion disease × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
656	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Prion disease × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 656. Prion disease × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
657	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Prion disease × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 657. Prion disease × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
658	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Prion disease × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 657. Prion disease × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
659	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Prion disease × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 659. Prion disease × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
660	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Prion disease × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 660. Prion disease × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
661	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Prion disease × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 661. Prion disease × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
662	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Prion disease × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 661. Prion disease × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
663	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Prion disease × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 663. Prion disease × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
664	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Prion disease × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 663. Prion disease × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
665	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Prion disease × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 665. Prion disease × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
666	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Prion disease × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 666. Prion disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
667	Prion disease 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Prion disease × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 666. Prion disease × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
668	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Renin secretion × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 668. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
669	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Renin secretion × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 668. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
670	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Renin secretion × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 668. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
671	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Renin secretion × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 668. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
672	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Renin secretion × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 672. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
673	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Renin secretion × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 672. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
674	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Renin secretion × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 674. Renin secretion × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
675	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Renin secretion × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 675. Renin secretion × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
676	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Renin secretion × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 676. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
677	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Renin secretion × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 676. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
678	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Renin secretion × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 676. Renin secretion × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
679	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Renin secretion × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 679. Renin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
680	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Renin secretion × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 680. Renin secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
681	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Renin secretion × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 680. Renin secretion × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
682	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Renin secretion × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 682. Renin secretion × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
683	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Renin secretion × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 683. Renin secretion × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
684	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Renin secretion × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 684. Renin secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
685	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Renin secretion × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 684. Renin secretion × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
686	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Renin secretion × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 686. Renin secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
687	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Renin secretion × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 686. Renin secretion × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
688	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Renin secretion × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 688. Renin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
689	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Renin secretion × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 689. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
690	Renin secretion 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Renin secretion × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 689. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
691	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Retrograde endocannabinoid signaling × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 691. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
692	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Retrograde endocannabinoid signaling × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 691. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
693	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Retrograde endocannabinoid signaling × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 691. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
694	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Retrograde endocannabinoid signaling × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 691. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
695	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 695. Retrograde endocannabinoid signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
696	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Retrograde endocannabinoid signaling × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 695. Retrograde endocannabinoid signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
697	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 697. Retrograde endocannabinoid signaling × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
698	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Retrograde endocannabinoid signaling × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 698. Retrograde endocannabinoid signaling × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
699	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 699. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
700	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Retrograde endocannabinoid signaling × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 699. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
701	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Retrograde endocannabinoid signaling × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 699. Retrograde endocannabinoid signaling × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
702	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Retrograde endocannabinoid signaling × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 702. Retrograde endocannabinoid signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
703	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 703. Retrograde endocannabinoid signaling × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
704	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Retrograde endocannabinoid signaling × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 703. Retrograde endocannabinoid signaling × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
705	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Retrograde endocannabinoid signaling × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 705. Retrograde endocannabinoid signaling × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
706	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Retrograde endocannabinoid signaling × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 706. Retrograde endocannabinoid signaling × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
707	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Retrograde endocannabinoid signaling × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 707. Retrograde endocannabinoid signaling × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
708	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Retrograde endocannabinoid signaling × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 707. Retrograde endocannabinoid signaling × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
709	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 709. Retrograde endocannabinoid signaling × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
710	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Retrograde endocannabinoid signaling × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 709. Retrograde endocannabinoid signaling × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
711	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Retrograde endocannabinoid signaling × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 711. Retrograde endocannabinoid signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
712	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Retrograde endocannabinoid signaling × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 712. Retrograde endocannabinoid signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
713	Retrograde endocannabinoid signaling 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Retrograde endocannabinoid signaling × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 712. Retrograde endocannabinoid signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
714	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Serotonergic synapse × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 714. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
715	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Serotonergic synapse × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 714. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
716	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Serotonergic synapse × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 714. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
717	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Serotonergic synapse × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 714. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
718	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Serotonergic synapse × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 718. Serotonergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
719	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Serotonergic synapse × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 718. Serotonergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
720	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Serotonergic synapse × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 720. Serotonergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
721	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Serotonergic synapse × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 721. Serotonergic synapse × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
722	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Serotonergic synapse × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 722. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
723	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Serotonergic synapse × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 722. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
724	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Serotonergic synapse × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 722. Serotonergic synapse × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
725	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Serotonergic synapse × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 725. Serotonergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
726	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Serotonergic synapse × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 726. Serotonergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
727	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Serotonergic synapse × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 726. Serotonergic synapse × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
728	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Serotonergic synapse × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 728. Serotonergic synapse × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
729	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Serotonergic synapse × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 729. Serotonergic synapse × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
730	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Serotonergic synapse × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 730. Serotonergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
731	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Serotonergic synapse × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 730. Serotonergic synapse × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
732	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Serotonergic synapse × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 732. Serotonergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
733	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Serotonergic synapse × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 732. Serotonergic synapse × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
734	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Serotonergic synapse × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 734. Serotonergic synapse × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
735	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Serotonergic synapse × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 735. Serotonergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
736	Serotonergic synapse 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Serotonergic synapse × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 735. Serotonergic synapse × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
737	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Tight junction × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 737. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
738	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Tight junction × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 737. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
739	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Tight junction × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 737. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
740	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Tight junction × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 737. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
741	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Tight junction × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 741. Tight junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
742	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Tight junction × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 741. Tight junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
743	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Tight junction × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 743. Tight junction × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
744	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Tight junction × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 744. Tight junction × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
745	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Tight junction × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 745. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
746	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Tight junction × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 745. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
747	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Tight junction × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 745. Tight junction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
748	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Tight junction × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 748. Tight junction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
749	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Tight junction × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 749. Tight junction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
750	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Tight junction × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 749. Tight junction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
751	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Tight junction × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 751. Tight junction × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
752	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Tight junction × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 752. Tight junction × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
753	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Tight junction × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 753. Tight junction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
754	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Tight junction × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 753. Tight junction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
755	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Tight junction × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 755. Tight junction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
756	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Tight junction × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 755. Tight junction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
757	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Tight junction × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 757. Tight junction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
758	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Tight junction × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 758. Tight junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
759	Tight junction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Tight junction × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 758. Tight junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
760	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Type II diabetes mellitus × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 760. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
761	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Type II diabetes mellitus × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 760. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
762	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Type II diabetes mellitus × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 760. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
763	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Type II diabetes mellitus × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 760. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
764	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Type II diabetes mellitus × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 764. Type II diabetes mellitus × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
765	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Type II diabetes mellitus × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 764. Type II diabetes mellitus × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
766	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Type II diabetes mellitus × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 766. Type II diabetes mellitus × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
767	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Type II diabetes mellitus × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 767. Type II diabetes mellitus × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
768	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Type II diabetes mellitus × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 768. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
769	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Type II diabetes mellitus × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 768. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
770	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Type II diabetes mellitus × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 768. Type II diabetes mellitus × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
771	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Type II diabetes mellitus × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 771. Type II diabetes mellitus × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
772	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Type II diabetes mellitus × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 772. Type II diabetes mellitus × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
773	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Type II diabetes mellitus × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 772. Type II diabetes mellitus × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
774	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Type II diabetes mellitus × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 774. Type II diabetes mellitus × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
775	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Type II diabetes mellitus × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 775. Type II diabetes mellitus × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
776	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Type II diabetes mellitus × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 776. Type II diabetes mellitus × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
777	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Type II diabetes mellitus × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 776. Type II diabetes mellitus × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
778	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Type II diabetes mellitus × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 778. Type II diabetes mellitus × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
779	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Type II diabetes mellitus × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 778. Type II diabetes mellitus × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
780	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Type II diabetes mellitus × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 780. Type II diabetes mellitus × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
781	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Type II diabetes mellitus × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 781. Type II diabetes mellitus × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
782	Type II diabetes mellitus 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Type II diabetes mellitus × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 781. Type II diabetes mellitus × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
783	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine besylate 💬 Vascular smooth muscle contraction × Name Other Names Amlodipine besylate Amlodipine besilate Norvasc NORLIQVA SDAMLO	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 783. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
784	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine maleate 💬 Vascular smooth muscle contraction × Name Other Names Amlodipine maleate Amvaz	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 783. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
785	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine 💬 Vascular smooth muscle contraction × Name Other Names Amlodipine Norvasc	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 783. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
786	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Amlodipine benzoate 💬 Vascular smooth muscle contraction × Name Other Names Amlodipine benzoate Katerzia	Amlodipine	[6] 51, 67, 79, 113, 222, 298 💬 783. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD; 79 Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia; 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis; 298 Hereditary pancreatitis;Chronic pancreatitis;
787	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Benidipine hydrochloride KW 3049 Coniel	Benidipine	[1] 57 💬 787. Vascular smooth muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
788	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Benidipine 💬 Vascular smooth muscle contraction × Name Other Names Benidipine Benidipine	Benidipine	[1] 57 💬 787. Vascular smooth muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
789	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Bevantolol hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Bevantolol hydrochloride Calvan Vantol	Bevantolol	[1]  8  💬 789. Vascular smooth muscle contraction × Disease ID Name  8  Huntington disease;Huntington chorea;Huntington syndrome;
790	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Cilnidipine 💬 Vascular smooth muscle contraction × Name Other Names Cilnidipine Atelec	Cilnidipine	[1] 67 💬 790. Vascular smooth muscle contraction × Disease ID Name 67 Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
791	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Diltiazem hydrochloride Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER	Diltiazem	[4] 51, 58, 86, 88 💬 791. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
792	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem malate 💬 Vascular smooth muscle contraction × Name Other Names Diltiazem malate Tiamate	Diltiazem	[4] 51, 58, 86, 88 💬 791. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
793	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Diltiazem 💬 Vascular smooth muscle contraction × Name Other Names Diltiazem Surazem	Diltiazem	[4] 51, 58, 86, 88 💬 791. Vascular smooth muscle contraction × Disease ID Name 51 Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 88 Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;
794	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Isradipine 💬 Vascular smooth muscle contraction × Name Other Names Isradipine Dynacirc	Isradipine	[1]  6  💬 794. Vascular smooth muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
795	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Nicardipine hydrochloride Cardene CARDENE IV NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE	Nicardipine	[2] 70, 86 💬 795. Vascular smooth muscle contraction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
796	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nicardipine 💬 Vascular smooth muscle contraction × Name Other Names Nicardipine Cardene	Nicardipine	[2] 70, 86 💬 795. Vascular smooth muscle contraction × Disease ID Name 70 Spinal stenosis;Extensive spinal canal stenosis; 86 Pulmonary arterial hypertension;PAH;
797	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nifedipine 💬 Vascular smooth muscle contraction × Name Other Names Nifedipine Adalat Afeditab CR Procardia	Nifedipine	[2] 50, 81 💬 797. Vascular smooth muscle contraction × Disease ID Name 50 Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM; 81 Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;
798	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Nilvadipine 💬 Vascular smooth muscle contraction × Name Other Names Nilvadipine Nivadil	Nilvadipine	[1] 90 💬 798. Vascular smooth muscle contraction × Disease ID Name 90 Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
799	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline maleate 💬 Vascular smooth muscle contraction × Name Other Names Perhexiline maleate Perhexiline maleate	Perhexiline	[2] 58, 272 💬 799. Vascular smooth muscle contraction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
800	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Perhexiline 💬 Vascular smooth muscle contraction × Name Other Names Perhexiline Perhexiline	Perhexiline	[2] 58, 272 💬 799. Vascular smooth muscle contraction × Disease ID Name 58 Hypertrophic cardiomyopathy;HCM; 272 Fibrodysplasia ossificans progressiva;FOP;
801	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Propiverine hydrochloride Bup-4 Mictonorm	Propiverine	[1] 226 💬 801. Vascular smooth muscle contraction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
802	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Propiverine 💬 Vascular smooth muscle contraction × Name Other Names Propiverine Propiverine	Propiverine	[1] 226 💬 801. Vascular smooth muscle contraction × Disease ID Name 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
803	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Topiramate 💬 Vascular smooth muscle contraction × Name Other Names Topiramate Topamax Trokendi xr EPRONTIA QUDEXY	Topiramate	[6]  6 , 97, 140, 144, 156, 193 💬 803. Vascular smooth muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 144 Lennox-Gastaut syndrome; 156 Rett syndrome; 193 Prader-Willi syndrome;
804	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil hydrochloride 💬 Vascular smooth muscle contraction × Name Other Names Verapamil hydrochloride Calan Covera-hs Vasolan Verelan VERAPAMIL HCI	Verapamil	[5] 57, 58, 96, 140, 167 💬 804. Vascular smooth muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;
805	Vascular smooth muscle contraction 💬	[1] CACNA1D 💬 Adrenergic signaling in cardiomyocytes × Name Full Name CACNA1D voltage-dependent L-type calcium channel subunit alpha-1D isoform b	Verapamil 💬 Vascular smooth muscle contraction × Name Other Names Verapamil Verapamil	Verapamil	[5] 57, 58, 96, 140, 167 💬 804. Vascular smooth muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM; 58 Hypertrophic cardiomyopathy;HCM; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 140 Dorabe syndrome;Dravet syndrome; 167 Marfan syndrome;Loeys-Dietz syndrome;LDS;

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