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 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
2	Adrenergic signaling in cardiomyocytes 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
3	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 3. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
4	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 3. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
5	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 3. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
6	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 6. Adrenergic signaling in cardiomyocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
7	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 6. Adrenergic signaling in cardiomyocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
8	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 6. Adrenergic signaling in cardiomyocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
9	Adrenergic signaling in cardiomyocytes 💬	[1] ADRB1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 6. Adrenergic signaling in cardiomyocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
10	Adrenergic signaling in cardiomyocytes 💬	[1] AGTR1 💬 Adrenergic signaling in cardiomyocytes × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 10. Adrenergic signaling in cardiomyocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
11	AGE-RAGE signaling pathway in diabetic complications 💬	[1] AGTR1 💬 AGE-RAGE signaling pathway in diabetic complications × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 AGE-RAGE signaling pathway in diabetic complications × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 11. AGE-RAGE signaling pathway in diabetic complications × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
12	Aldosterone synthesis and secretion 💬	[1] AGTR1 💬 Aldosterone synthesis and secretion × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Aldosterone synthesis and secretion × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 12. Aldosterone synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
13	AMPK signaling pathway 💬	[1] ADRA1A 💬 AMPK signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A	Carvedilol 💬 AMPK signaling pathway × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 13. AMPK signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
14	AMPK signaling pathway 💬	[1] ADRA1A 💬 AMPK signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A	Carvedilol phosphate 💬 AMPK signaling pathway × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 13. AMPK signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
15	Apelin signaling pathway 💬	[1] AGTR1 💬 Apelin signaling pathway × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Apelin signaling pathway × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 15. Apelin signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
16	Caffeine metabolism 💬	[1] XDH 💬 Caffeine metabolism × Name Full Name XDH xanthine dehydrogenase	Allopurinol 💬 Caffeine metabolism × Name Other Names Allopurinol Allopurinol (JP18/USP/INN) Zyloprim (TN) ALLOPURINOL	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 16. Caffeine metabolism × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
17	Caffeine metabolism 💬	[1] XDH 💬 Caffeine metabolism × Name Full Name XDH xanthine dehydrogenase	Allopurinol sodium 💬 Caffeine metabolism × Name Other Names Allopurinol sodium Allopurinol sodium Aloprim (TN) ALOPRIM ALLOPURINOL ALLOPURINOL SODIUM	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 16. Caffeine metabolism × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
18	Calcium signaling pathway 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Calcium signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Calcium signaling pathway × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 18. Calcium signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
19	Calcium signaling pathway 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Calcium signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Calcium signaling pathway × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 18. Calcium signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
20	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Calcium signaling pathway × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 20. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
21	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Calcium signaling pathway × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 20. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
22	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Calcium signaling pathway × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 20. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
23	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Calcium signaling pathway × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 23. Calcium signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
24	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Calcium signaling pathway × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 23. Calcium signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
25	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Calcium signaling pathway × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 23. Calcium signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
26	Calcium signaling pathway 💬	[1] ADRB1 💬 Calcium signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Calcium signaling pathway × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 23. Calcium signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
27	Calcium signaling pathway 💬	[1] AGTR1 💬 Calcium signaling pathway × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Calcium signaling pathway × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 27. Calcium signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
28	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 cAMP signaling pathway × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 28. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
29	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 cAMP signaling pathway × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 28. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
30	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 cAMP signaling pathway × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 28. cAMP signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
31	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 cAMP signaling pathway × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 31. cAMP signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
32	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 cAMP signaling pathway × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 31. cAMP signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
33	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 cAMP signaling pathway × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 31. cAMP signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
34	cAMP signaling pathway 💬	[1] ADRB1 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 cAMP signaling pathway × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 31. cAMP signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
35	cAMP signaling pathway 💬	[2] ADRB1, ADRB2 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 cAMP signaling pathway × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 35. cAMP signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
36	cAMP signaling pathway 💬	[2] ADRB1, ADRB2 💬 cAMP signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 cAMP signaling pathway × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 35. cAMP signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
37	cGMP-PKG signaling pathway 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 cGMP-PKG signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 cGMP-PKG signaling pathway × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 37. cGMP-PKG signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
38	cGMP-PKG signaling pathway 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 cGMP-PKG signaling pathway × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 cGMP-PKG signaling pathway × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 37. cGMP-PKG signaling pathway × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
39	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 cGMP-PKG signaling pathway × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 39. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
40	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 cGMP-PKG signaling pathway × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 39. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
41	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 cGMP-PKG signaling pathway × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 39. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
42	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 cGMP-PKG signaling pathway × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 42. cGMP-PKG signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
43	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 cGMP-PKG signaling pathway × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 42. cGMP-PKG signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
44	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 cGMP-PKG signaling pathway × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 42. cGMP-PKG signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
45	cGMP-PKG signaling pathway 💬	[1] ADRB1 💬 cGMP-PKG signaling pathway × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 cGMP-PKG signaling pathway × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 42. cGMP-PKG signaling pathway × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
46	cGMP-PKG signaling pathway 💬	[1] AGTR1 💬 cGMP-PKG signaling pathway × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 cGMP-PKG signaling pathway × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 46. cGMP-PKG signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
47	Chagas disease 💬	[1] ACE 💬 Chagas disease × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Chagas disease × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 47. Chagas disease × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
48	Chagas disease 💬	[1] ACE 💬 Chagas disease × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Chagas disease × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 47. Chagas disease × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
49	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Chemical carcinogenesis - receptor activation × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 49. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
50	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Chemical carcinogenesis - receptor activation × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 49. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
51	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 49. Chemical carcinogenesis - receptor activation × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
52	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 52. Chemical carcinogenesis - receptor activation × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
53	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 52. Chemical carcinogenesis - receptor activation × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
54	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Chemical carcinogenesis - receptor activation × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 52. Chemical carcinogenesis - receptor activation × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
55	Chemical carcinogenesis - receptor activation 💬	[1] ADRB1 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 52. Chemical carcinogenesis - receptor activation × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
56	Chemical carcinogenesis - receptor activation 💬	[2] ADRB1, ADRB2 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Chemical carcinogenesis - receptor activation × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 56. Chemical carcinogenesis - receptor activation × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
57	Chemical carcinogenesis - receptor activation 💬	[2] ADRB1, ADRB2 💬 Chemical carcinogenesis - receptor activation × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Chemical carcinogenesis - receptor activation × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 56. Chemical carcinogenesis - receptor activation × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
58	Coronavirus disease - COVID-19 💬	[1] ACE 💬 Coronavirus disease - COVID-19 × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Coronavirus disease - COVID-19 × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 58. Coronavirus disease - COVID-19 × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
59	Coronavirus disease - COVID-19 💬	[1] ACE 💬 Coronavirus disease - COVID-19 × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Coronavirus disease - COVID-19 × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 58. Coronavirus disease - COVID-19 × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
60	Coronavirus disease - COVID-19 💬	[1] AGTR1 💬 Coronavirus disease - COVID-19 × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Coronavirus disease - COVID-19 × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 60. Coronavirus disease - COVID-19 × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
61	Cortisol synthesis and secretion 💬	[1] AGTR1 💬 Cortisol synthesis and secretion × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Cortisol synthesis and secretion × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 61. Cortisol synthesis and secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
62	Cushing syndrome 💬	[1] AGTR1 💬 Cushing syndrome × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Cushing syndrome × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 62. Cushing syndrome × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
63	Cytokine-cytokine receptor interaction 💬	[1] CSF3R 💬 Cytokine-cytokine receptor interaction × Name Full Name CSF3R colony stimulating factor 3 receptor	Lenograstim 💬 Cytokine-cytokine receptor interaction × Name Other Names Lenograstim Lenograstim (USAN/INN) Lenograstim (genetical recombination) (JP18) Neutrogin (TN)	Lenograstim	[8]  2 , 13, 16, 18, 19, 57, 65, 97 💬 63. Cytokine-cytokine receptor interaction × Disease ID Name  2  Amyotrophic lateral sclerosis;ALS; 13 Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis; 16 Crow-Fukase syndrome;Polyneuropathy, organomegaly, endocrinopathy, m-protein, and skin changes syndrome;POEMS syndrome;Takatsuki disease;Polyneuropathy, endocrinopathy, plasma cell dyscrasia syndrome;PEP syndrome; 18 Spinocerebellar degeneration;SCD;:Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysial atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;Neu:Ataxia with vitamin E deficiency;AVED;Aprataxin deficiency;APTX deficiency;Friedreich ataxia;FRDA;Senataxin deficiency;SETX deficiency;Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Spastic ataxia; 19 Lysosomal storage disease;Lysosomal disease;Gaucher disease;Niemann-Pick disease type A/B;Niemann-Pick type A;NPD-A;NPA;Niemann-Pick type B;NPD-B;NPB;Acid sphingomyelinase deficiency;ASMD;Niemann-Pick disease type C;Niemann-Pick type C;NPD-C;NPC;GM1-gangliosidosis;GM1-gangliosidoses;GM2-gangliosidosis;GM2-gangliosidoses;Tay-Sachs disease;Sandhoff disease;Krabbe disease;Metachromatic leukodystrophy;MLD;Multiple-sulfatase deficiency;Farber disease;Mucopolysaccharidosis type I;Mucopolysaccharidosis I;MPS I;Hurler syndrome;Hurler-Scheie syndrome;Scheie syndrome;Mucopolysaccharidosis type II;Mucopolysaccharidosis II;MPS II;Hunter syndrome;Mucopolysaccharidosis type III;Mucopolysaccharidosis III;MPS III;Sanfilippo syndrome;Mucopolysaccharidosis type IV;Mucopolysaccharidosis IV;MPS IV;MPS IVA;Morquio syndrome;Morquio A syndrome;Mucopolysaccharidosis type VI;Mucopolysaccharidosis VI;MPS VI;Maroteaux-Lamy syndrome;Mucopolysaccharidosis type VII;Mucopolysaccharidosis VII;MPS VII;Sly syndrome;Mucopolysaccharidosis type IX;Mucopolysaccharidosis IX;MPS IX;Hyaluronidase deficiency;Sialidosis;Galactosialidosis;Mucolipidosis II;Mucolipidosis type II;I-cell disease;Mucolipidosis III;Mucolipidosis type III;Alpha-Mannosidosis;Alpha-Mannosidase Deficiency;Beta-Mannosidosis;Beta-Mannosidase Deficiency;Fucosidosis;Aspartylglucosaminuria;Schindler disease;Kanzaki disease;Pompe disease;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Ceroid lipofuscinosis;Fabry disease;Cystinosis; 57 Idiopathic dilated cardiomyopathy; 65 Primary immunodeficiency;X-linked severe combined immunodeficiency;X-SCID;Reticular dysgenesis;Adenosine deaminase deficiency;Omenn syndrome;Purine nucleoside phosphorylase deficiency;CD8 deficiency;ZAP-70 deficiency;MHC class I deficiency;MHC class II deficiency;Other combined immunodeficiencies;Wiskott-Aldrich syndrome;WAS;Ataxia telangiectasia;Nijmegen breakage syndrome;Bloom syndrome;Immunodeficiency, centromere region instability, facial anomalies syndrome;ICF syndrome;PMS2 deficiency;Radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties syndrome;RIDDLE syndrome;Schimke syndrome;Netherton syndrome;Thymic hypoplasia;DiGeorge syndrome;22q11.2 deletion syndrome;Hyper-IgE syndrome;Hepatic venoocclusive immunodeficiency;Immunodeficiency with central hepatic vein atresia;Dyskeratosis congenita;X-linked agammaglobulinaemia;Common variable immunodeficiency;Hyper-IgM syndrome;Isolated IgG subclass deficiency;Selective IgA deficiency;Specific antibody production deficiency;Infant transient hypogammaglobulinemia;Other predominantly antibody deficiencies;Chédiak-Higashi syndrome;Chediak-Higashi syndrome;X-linked lymphoproliferative syndrome;SAP deficiency;SH2D1A/SLAM-associated protein deficiency;XIAP deficiency;X-linked inhibitor of apoptosis deficiency;Autoimmune lymphoproliferative syndrome;ALPS;Other diseases of immune dysregulation;Familial hemophagocytic syndrome;FHPS;Familial hemophagocytic lymphohistiocytosis;FHL;Perforin deficiency;Munc13-4 deficiency;Syntaxin 11 deficiency;Munc18-2 deficiency;Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy;APECED;Autoimmune polyglandular syndrome;APS;Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome;IPEX syndrome;CD25 deficiency;ITCH deficiency;Severe congenital neutropenia;Cyclic neutropenia;Other congenital defects of neutrophil function;p14 deficiency;Glycogen storage disease type Ib;Leukocyte adhesion deficiency;Shwachman-Diamond syndrome;Chronic granulomatous disease;Myeloperoxidase deficiency;Mendelian susceptibility to mycobacterial disease;MSMD;Other congenital defects of phagocyte function;Anhidrotic ectodermal dysplasia with immunodeficiency;EDA-ID;Interleukin-1 receptor-associated kinase-4 deficiency;IRAK4 deficiency;MyD88 deficiency;Chronic mucocutaneous candidiasis;Other defects in innate immunity;Warts, hypogammaglobulinemia, infections, myelokathexis syndrome;WHIM syndrome;Congenital complement deficiency;C1q deficiency;C1r deficiency;C1s deficiency;C2 deficiency;C3 deficiency;C4 deficiency;C5 deficiency;C6 deficiency;C7 deficiency;C8 deficiency;C9 deficiency;Hereditary angioedema;C1 inhibitor deficiency;Inherited deficiency of complement system;Factor D deficiency;Factor I deficiency;Factor H deficiency;Properdin deficiency;MASP1 deficiency;MASP2 deficiency;3MC syndrome;Immunodeficiency associated with FCN3 mutation;FCN3; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
64	Diabetic cardiomyopathy 💬	[1] ACE 💬 Diabetic cardiomyopathy × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Diabetic cardiomyopathy × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 64. Diabetic cardiomyopathy × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
65	Diabetic cardiomyopathy 💬	[1] ACE 💬 Diabetic cardiomyopathy × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Diabetic cardiomyopathy × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 64. Diabetic cardiomyopathy × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
66	Diabetic cardiomyopathy 💬	[1] AGTR1 💬 Diabetic cardiomyopathy × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Diabetic cardiomyopathy × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 66. Diabetic cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
67	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Carvedilol 💬 Dilated cardiomyopathy × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 67. Dilated cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
68	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Carvedilol phosphate 💬 Dilated cardiomyopathy × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 67. Dilated cardiomyopathy × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
69	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Dilated cardiomyopathy × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 69. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
70	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Dilated cardiomyopathy × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 69. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
71	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Dilated cardiomyopathy × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 69. Dilated cardiomyopathy × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
72	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Dilated cardiomyopathy × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 72. Dilated cardiomyopathy × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
73	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Dilated cardiomyopathy × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 72. Dilated cardiomyopathy × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
74	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Dilated cardiomyopathy × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 72. Dilated cardiomyopathy × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
75	Dilated cardiomyopathy 💬	[1] ADRB1 💬 Dilated cardiomyopathy × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Dilated cardiomyopathy × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 72. Dilated cardiomyopathy × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
76	Drug metabolism - other enzymes 💬	[1] XDH 💬 Drug metabolism - other enzymes × Name Full Name XDH xanthine dehydrogenase	Allopurinol 💬 Drug metabolism - other enzymes × Name Other Names Allopurinol Allopurinol (JP18/USP/INN) Zyloprim (TN) ALLOPURINOL	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 76. Drug metabolism - other enzymes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
77	Drug metabolism - other enzymes 💬	[1] XDH 💬 Drug metabolism - other enzymes × Name Full Name XDH xanthine dehydrogenase	Allopurinol sodium 💬 Drug metabolism - other enzymes × Name Other Names Allopurinol sodium Allopurinol sodium Aloprim (TN) ALOPRIM ALLOPURINOL ALLOPURINOL SODIUM	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 76. Drug metabolism - other enzymes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
78	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Carvedilol 💬 Gap junction × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 78. Gap junction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
79	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Carvedilol phosphate 💬 Gap junction × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 78. Gap junction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
80	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Gap junction × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 80. Gap junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
81	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Gap junction × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 80. Gap junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
82	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Gap junction × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 80. Gap junction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
83	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Gap junction × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 83. Gap junction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
84	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Gap junction × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 83. Gap junction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
85	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Gap junction × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 83. Gap junction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
86	Gap junction 💬	[1] ADRB1 💬 Gap junction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Gap junction × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 83. Gap junction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
87	Hematopoietic cell lineage 💬	[1] CSF3R 💬 Hematopoietic cell lineage × Name Full Name CSF3R colony stimulating factor 3 receptor	Lenograstim 💬 Hematopoietic cell lineage × Name Other Names Lenograstim Lenograstim (USAN/INN) Lenograstim (genetical recombination) (JP18) Neutrogin (TN)	Lenograstim	[8]  2 , 13, 16, 18, 19, 57, 65, 97 💬 87. Hematopoietic cell lineage × Disease ID Name  2  Amyotrophic lateral sclerosis;ALS; 13 Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis; 16 Crow-Fukase syndrome;Polyneuropathy, organomegaly, endocrinopathy, m-protein, and skin changes syndrome;POEMS syndrome;Takatsuki disease;Polyneuropathy, endocrinopathy, plasma cell dyscrasia syndrome;PEP syndrome; 18 Spinocerebellar degeneration;SCD;:Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysial atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;Neu:Ataxia with vitamin E deficiency;AVED;Aprataxin deficiency;APTX deficiency;Friedreich ataxia;FRDA;Senataxin deficiency;SETX deficiency;Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Spastic ataxia; 19 Lysosomal storage disease;Lysosomal disease;Gaucher disease;Niemann-Pick disease type A/B;Niemann-Pick type A;NPD-A;NPA;Niemann-Pick type B;NPD-B;NPB;Acid sphingomyelinase deficiency;ASMD;Niemann-Pick disease type C;Niemann-Pick type C;NPD-C;NPC;GM1-gangliosidosis;GM1-gangliosidoses;GM2-gangliosidosis;GM2-gangliosidoses;Tay-Sachs disease;Sandhoff disease;Krabbe disease;Metachromatic leukodystrophy;MLD;Multiple-sulfatase deficiency;Farber disease;Mucopolysaccharidosis type I;Mucopolysaccharidosis I;MPS I;Hurler syndrome;Hurler-Scheie syndrome;Scheie syndrome;Mucopolysaccharidosis type II;Mucopolysaccharidosis II;MPS II;Hunter syndrome;Mucopolysaccharidosis type III;Mucopolysaccharidosis III;MPS III;Sanfilippo syndrome;Mucopolysaccharidosis type IV;Mucopolysaccharidosis IV;MPS IV;MPS IVA;Morquio syndrome;Morquio A syndrome;Mucopolysaccharidosis type VI;Mucopolysaccharidosis VI;MPS VI;Maroteaux-Lamy syndrome;Mucopolysaccharidosis type VII;Mucopolysaccharidosis VII;MPS VII;Sly syndrome;Mucopolysaccharidosis type IX;Mucopolysaccharidosis IX;MPS IX;Hyaluronidase deficiency;Sialidosis;Galactosialidosis;Mucolipidosis II;Mucolipidosis type II;I-cell disease;Mucolipidosis III;Mucolipidosis type III;Alpha-Mannosidosis;Alpha-Mannosidase Deficiency;Beta-Mannosidosis;Beta-Mannosidase Deficiency;Fucosidosis;Aspartylglucosaminuria;Schindler disease;Kanzaki disease;Pompe disease;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Ceroid lipofuscinosis;Fabry disease;Cystinosis; 57 Idiopathic dilated cardiomyopathy; 65 Primary immunodeficiency;X-linked severe combined immunodeficiency;X-SCID;Reticular dysgenesis;Adenosine deaminase deficiency;Omenn syndrome;Purine nucleoside phosphorylase deficiency;CD8 deficiency;ZAP-70 deficiency;MHC class I deficiency;MHC class II deficiency;Other combined immunodeficiencies;Wiskott-Aldrich syndrome;WAS;Ataxia telangiectasia;Nijmegen breakage syndrome;Bloom syndrome;Immunodeficiency, centromere region instability, facial anomalies syndrome;ICF syndrome;PMS2 deficiency;Radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties syndrome;RIDDLE syndrome;Schimke syndrome;Netherton syndrome;Thymic hypoplasia;DiGeorge syndrome;22q11.2 deletion syndrome;Hyper-IgE syndrome;Hepatic venoocclusive immunodeficiency;Immunodeficiency with central hepatic vein atresia;Dyskeratosis congenita;X-linked agammaglobulinaemia;Common variable immunodeficiency;Hyper-IgM syndrome;Isolated IgG subclass deficiency;Selective IgA deficiency;Specific antibody production deficiency;Infant transient hypogammaglobulinemia;Other predominantly antibody deficiencies;Chédiak-Higashi syndrome;Chediak-Higashi syndrome;X-linked lymphoproliferative syndrome;SAP deficiency;SH2D1A/SLAM-associated protein deficiency;XIAP deficiency;X-linked inhibitor of apoptosis deficiency;Autoimmune lymphoproliferative syndrome;ALPS;Other diseases of immune dysregulation;Familial hemophagocytic syndrome;FHPS;Familial hemophagocytic lymphohistiocytosis;FHL;Perforin deficiency;Munc13-4 deficiency;Syntaxin 11 deficiency;Munc18-2 deficiency;Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy;APECED;Autoimmune polyglandular syndrome;APS;Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome;IPEX syndrome;CD25 deficiency;ITCH deficiency;Severe congenital neutropenia;Cyclic neutropenia;Other congenital defects of neutrophil function;p14 deficiency;Glycogen storage disease type Ib;Leukocyte adhesion deficiency;Shwachman-Diamond syndrome;Chronic granulomatous disease;Myeloperoxidase deficiency;Mendelian susceptibility to mycobacterial disease;MSMD;Other congenital defects of phagocyte function;Anhidrotic ectodermal dysplasia with immunodeficiency;EDA-ID;Interleukin-1 receptor-associated kinase-4 deficiency;IRAK4 deficiency;MyD88 deficiency;Chronic mucocutaneous candidiasis;Other defects in innate immunity;Warts, hypogammaglobulinemia, infections, myelokathexis syndrome;WHIM syndrome;Congenital complement deficiency;C1q deficiency;C1r deficiency;C1s deficiency;C2 deficiency;C3 deficiency;C4 deficiency;C5 deficiency;C6 deficiency;C7 deficiency;C8 deficiency;C9 deficiency;Hereditary angioedema;C1 inhibitor deficiency;Inherited deficiency of complement system;Factor D deficiency;Factor I deficiency;Factor H deficiency;Properdin deficiency;MASP1 deficiency;MASP2 deficiency;3MC syndrome;Immunodeficiency associated with FCN3 mutation;FCN3; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
88	Hormone signaling 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Hormone signaling × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Hormone signaling × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 88. Hormone signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
89	Hormone signaling 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Hormone signaling × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Hormone signaling × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 88. Hormone signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
90	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Hormone signaling × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 90. Hormone signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
91	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Hormone signaling × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 90. Hormone signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
92	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Hormone signaling × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 90. Hormone signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
93	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Hormone signaling × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 93. Hormone signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
94	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Hormone signaling × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 93. Hormone signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
95	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Hormone signaling × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 93. Hormone signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
96	Hormone signaling 💬	[1] ADRB1 💬 Hormone signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Hormone signaling × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 93. Hormone signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
97	Hormone signaling 💬	[1] AGTR1 💬 Hormone signaling × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Hormone signaling × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 97. Hormone signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
98	Hypertrophic cardiomyopathy 💬	[1] ACE 💬 Hypertrophic cardiomyopathy × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Hypertrophic cardiomyopathy × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 98. Hypertrophic cardiomyopathy × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
99	Hypertrophic cardiomyopathy 💬	[1] ACE 💬 Hypertrophic cardiomyopathy × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Hypertrophic cardiomyopathy × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 98. Hypertrophic cardiomyopathy × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
100	JAK-STAT signaling pathway 💬	[1] CSF3R 💬 JAK-STAT signaling pathway × Name Full Name CSF3R colony stimulating factor 3 receptor	Lenograstim 💬 JAK-STAT signaling pathway × Name Other Names Lenograstim Lenograstim (USAN/INN) Lenograstim (genetical recombination) (JP18) Neutrogin (TN)	Lenograstim	[8]  2 , 13, 16, 18, 19, 57, 65, 97 💬 100. JAK-STAT signaling pathway × Disease ID Name  2  Amyotrophic lateral sclerosis;ALS; 13 Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis; 16 Crow-Fukase syndrome;Polyneuropathy, organomegaly, endocrinopathy, m-protein, and skin changes syndrome;POEMS syndrome;Takatsuki disease;Polyneuropathy, endocrinopathy, plasma cell dyscrasia syndrome;PEP syndrome; 18 Spinocerebellar degeneration;SCD;:Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysial atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;Neu:Ataxia with vitamin E deficiency;AVED;Aprataxin deficiency;APTX deficiency;Friedreich ataxia;FRDA;Senataxin deficiency;SETX deficiency;Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Spastic ataxia; 19 Lysosomal storage disease;Lysosomal disease;Gaucher disease;Niemann-Pick disease type A/B;Niemann-Pick type A;NPD-A;NPA;Niemann-Pick type B;NPD-B;NPB;Acid sphingomyelinase deficiency;ASMD;Niemann-Pick disease type C;Niemann-Pick type C;NPD-C;NPC;GM1-gangliosidosis;GM1-gangliosidoses;GM2-gangliosidosis;GM2-gangliosidoses;Tay-Sachs disease;Sandhoff disease;Krabbe disease;Metachromatic leukodystrophy;MLD;Multiple-sulfatase deficiency;Farber disease;Mucopolysaccharidosis type I;Mucopolysaccharidosis I;MPS I;Hurler syndrome;Hurler-Scheie syndrome;Scheie syndrome;Mucopolysaccharidosis type II;Mucopolysaccharidosis II;MPS II;Hunter syndrome;Mucopolysaccharidosis type III;Mucopolysaccharidosis III;MPS III;Sanfilippo syndrome;Mucopolysaccharidosis type IV;Mucopolysaccharidosis IV;MPS IV;MPS IVA;Morquio syndrome;Morquio A syndrome;Mucopolysaccharidosis type VI;Mucopolysaccharidosis VI;MPS VI;Maroteaux-Lamy syndrome;Mucopolysaccharidosis type VII;Mucopolysaccharidosis VII;MPS VII;Sly syndrome;Mucopolysaccharidosis type IX;Mucopolysaccharidosis IX;MPS IX;Hyaluronidase deficiency;Sialidosis;Galactosialidosis;Mucolipidosis II;Mucolipidosis type II;I-cell disease;Mucolipidosis III;Mucolipidosis type III;Alpha-Mannosidosis;Alpha-Mannosidase Deficiency;Beta-Mannosidosis;Beta-Mannosidase Deficiency;Fucosidosis;Aspartylglucosaminuria;Schindler disease;Kanzaki disease;Pompe disease;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Ceroid lipofuscinosis;Fabry disease;Cystinosis; 57 Idiopathic dilated cardiomyopathy; 65 Primary immunodeficiency;X-linked severe combined immunodeficiency;X-SCID;Reticular dysgenesis;Adenosine deaminase deficiency;Omenn syndrome;Purine nucleoside phosphorylase deficiency;CD8 deficiency;ZAP-70 deficiency;MHC class I deficiency;MHC class II deficiency;Other combined immunodeficiencies;Wiskott-Aldrich syndrome;WAS;Ataxia telangiectasia;Nijmegen breakage syndrome;Bloom syndrome;Immunodeficiency, centromere region instability, facial anomalies syndrome;ICF syndrome;PMS2 deficiency;Radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties syndrome;RIDDLE syndrome;Schimke syndrome;Netherton syndrome;Thymic hypoplasia;DiGeorge syndrome;22q11.2 deletion syndrome;Hyper-IgE syndrome;Hepatic venoocclusive immunodeficiency;Immunodeficiency with central hepatic vein atresia;Dyskeratosis congenita;X-linked agammaglobulinaemia;Common variable immunodeficiency;Hyper-IgM syndrome;Isolated IgG subclass deficiency;Selective IgA deficiency;Specific antibody production deficiency;Infant transient hypogammaglobulinemia;Other predominantly antibody deficiencies;Chédiak-Higashi syndrome;Chediak-Higashi syndrome;X-linked lymphoproliferative syndrome;SAP deficiency;SH2D1A/SLAM-associated protein deficiency;XIAP deficiency;X-linked inhibitor of apoptosis deficiency;Autoimmune lymphoproliferative syndrome;ALPS;Other diseases of immune dysregulation;Familial hemophagocytic syndrome;FHPS;Familial hemophagocytic lymphohistiocytosis;FHL;Perforin deficiency;Munc13-4 deficiency;Syntaxin 11 deficiency;Munc18-2 deficiency;Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy;APECED;Autoimmune polyglandular syndrome;APS;Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome;IPEX syndrome;CD25 deficiency;ITCH deficiency;Severe congenital neutropenia;Cyclic neutropenia;Other congenital defects of neutrophil function;p14 deficiency;Glycogen storage disease type Ib;Leukocyte adhesion deficiency;Shwachman-Diamond syndrome;Chronic granulomatous disease;Myeloperoxidase deficiency;Mendelian susceptibility to mycobacterial disease;MSMD;Other congenital defects of phagocyte function;Anhidrotic ectodermal dysplasia with immunodeficiency;EDA-ID;Interleukin-1 receptor-associated kinase-4 deficiency;IRAK4 deficiency;MyD88 deficiency;Chronic mucocutaneous candidiasis;Other defects in innate immunity;Warts, hypogammaglobulinemia, infections, myelokathexis syndrome;WHIM syndrome;Congenital complement deficiency;C1q deficiency;C1r deficiency;C1s deficiency;C2 deficiency;C3 deficiency;C4 deficiency;C5 deficiency;C6 deficiency;C7 deficiency;C8 deficiency;C9 deficiency;Hereditary angioedema;C1 inhibitor deficiency;Inherited deficiency of complement system;Factor D deficiency;Factor I deficiency;Factor H deficiency;Properdin deficiency;MASP1 deficiency;MASP2 deficiency;3MC syndrome;Immunodeficiency associated with FCN3 mutation;FCN3; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
101	Neuroactive ligand signaling 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Neuroactive ligand signaling × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Neuroactive ligand signaling × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 101. Neuroactive ligand signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
102	Neuroactive ligand signaling 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Neuroactive ligand signaling × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Neuroactive ligand signaling × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 101. Neuroactive ligand signaling × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
103	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Neuroactive ligand signaling × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 103. Neuroactive ligand signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
104	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Neuroactive ligand signaling × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 103. Neuroactive ligand signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
105	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Neuroactive ligand signaling × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 103. Neuroactive ligand signaling × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
106	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Neuroactive ligand signaling × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 106. Neuroactive ligand signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
107	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Neuroactive ligand signaling × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 106. Neuroactive ligand signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
108	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Neuroactive ligand signaling × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 106. Neuroactive ligand signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
109	Neuroactive ligand signaling 💬	[1] ADRB1 💬 Neuroactive ligand signaling × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Neuroactive ligand signaling × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 106. Neuroactive ligand signaling × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
110	Neuroactive ligand-receptor interaction 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Neuroactive ligand-receptor interaction × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 110. Neuroactive ligand-receptor interaction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
111	Neuroactive ligand-receptor interaction 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Neuroactive ligand-receptor interaction × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 110. Neuroactive ligand-receptor interaction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
112	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Neuroactive ligand-receptor interaction × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 112. Neuroactive ligand-receptor interaction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
113	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Neuroactive ligand-receptor interaction × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 112. Neuroactive ligand-receptor interaction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
114	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Neuroactive ligand-receptor interaction × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 112. Neuroactive ligand-receptor interaction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
115	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Neuroactive ligand-receptor interaction × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 115. Neuroactive ligand-receptor interaction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
116	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Neuroactive ligand-receptor interaction × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 115. Neuroactive ligand-receptor interaction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
117	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Neuroactive ligand-receptor interaction × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 115. Neuroactive ligand-receptor interaction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
118	Neuroactive ligand-receptor interaction 💬	[1] ADRB1 💬 Neuroactive ligand-receptor interaction × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Neuroactive ligand-receptor interaction × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 115. Neuroactive ligand-receptor interaction × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
119	Neuroactive ligand-receptor interaction 💬	[1] AGTR1 💬 Neuroactive ligand-receptor interaction × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Neuroactive ligand-receptor interaction × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 119. Neuroactive ligand-receptor interaction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
120	Pathways in cancer 💬	[1] AGTR1 💬 Pathways in cancer × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Pathways in cancer × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 120. Pathways in cancer × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
121	Pathways in cancer 💬	[1] CSF3R 💬 Pathways in cancer × Name Full Name CSF3R colony stimulating factor 3 receptor	Lenograstim 💬 Pathways in cancer × Name Other Names Lenograstim Lenograstim (USAN/INN) Lenograstim (genetical recombination) (JP18) Neutrogin (TN)	Lenograstim	[8]  2 , 13, 16, 18, 19, 57, 65, 97 💬 121. Pathways in cancer × Disease ID Name  2  Amyotrophic lateral sclerosis;ALS; 13 Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis; 16 Crow-Fukase syndrome;Polyneuropathy, organomegaly, endocrinopathy, m-protein, and skin changes syndrome;POEMS syndrome;Takatsuki disease;Polyneuropathy, endocrinopathy, plasma cell dyscrasia syndrome;PEP syndrome; 18 Spinocerebellar degeneration;SCD;:Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysial atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;Neu:Ataxia with vitamin E deficiency;AVED;Aprataxin deficiency;APTX deficiency;Friedreich ataxia;FRDA;Senataxin deficiency;SETX deficiency;Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Spastic ataxia; 19 Lysosomal storage disease;Lysosomal disease;Gaucher disease;Niemann-Pick disease type A/B;Niemann-Pick type A;NPD-A;NPA;Niemann-Pick type B;NPD-B;NPB;Acid sphingomyelinase deficiency;ASMD;Niemann-Pick disease type C;Niemann-Pick type C;NPD-C;NPC;GM1-gangliosidosis;GM1-gangliosidoses;GM2-gangliosidosis;GM2-gangliosidoses;Tay-Sachs disease;Sandhoff disease;Krabbe disease;Metachromatic leukodystrophy;MLD;Multiple-sulfatase deficiency;Farber disease;Mucopolysaccharidosis type I;Mucopolysaccharidosis I;MPS I;Hurler syndrome;Hurler-Scheie syndrome;Scheie syndrome;Mucopolysaccharidosis type II;Mucopolysaccharidosis II;MPS II;Hunter syndrome;Mucopolysaccharidosis type III;Mucopolysaccharidosis III;MPS III;Sanfilippo syndrome;Mucopolysaccharidosis type IV;Mucopolysaccharidosis IV;MPS IV;MPS IVA;Morquio syndrome;Morquio A syndrome;Mucopolysaccharidosis type VI;Mucopolysaccharidosis VI;MPS VI;Maroteaux-Lamy syndrome;Mucopolysaccharidosis type VII;Mucopolysaccharidosis VII;MPS VII;Sly syndrome;Mucopolysaccharidosis type IX;Mucopolysaccharidosis IX;MPS IX;Hyaluronidase deficiency;Sialidosis;Galactosialidosis;Mucolipidosis II;Mucolipidosis type II;I-cell disease;Mucolipidosis III;Mucolipidosis type III;Alpha-Mannosidosis;Alpha-Mannosidase Deficiency;Beta-Mannosidosis;Beta-Mannosidase Deficiency;Fucosidosis;Aspartylglucosaminuria;Schindler disease;Kanzaki disease;Pompe disease;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Ceroid lipofuscinosis;Fabry disease;Cystinosis; 57 Idiopathic dilated cardiomyopathy; 65 Primary immunodeficiency;X-linked severe combined immunodeficiency;X-SCID;Reticular dysgenesis;Adenosine deaminase deficiency;Omenn syndrome;Purine nucleoside phosphorylase deficiency;CD8 deficiency;ZAP-70 deficiency;MHC class I deficiency;MHC class II deficiency;Other combined immunodeficiencies;Wiskott-Aldrich syndrome;WAS;Ataxia telangiectasia;Nijmegen breakage syndrome;Bloom syndrome;Immunodeficiency, centromere region instability, facial anomalies syndrome;ICF syndrome;PMS2 deficiency;Radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties syndrome;RIDDLE syndrome;Schimke syndrome;Netherton syndrome;Thymic hypoplasia;DiGeorge syndrome;22q11.2 deletion syndrome;Hyper-IgE syndrome;Hepatic venoocclusive immunodeficiency;Immunodeficiency with central hepatic vein atresia;Dyskeratosis congenita;X-linked agammaglobulinaemia;Common variable immunodeficiency;Hyper-IgM syndrome;Isolated IgG subclass deficiency;Selective IgA deficiency;Specific antibody production deficiency;Infant transient hypogammaglobulinemia;Other predominantly antibody deficiencies;Chédiak-Higashi syndrome;Chediak-Higashi syndrome;X-linked lymphoproliferative syndrome;SAP deficiency;SH2D1A/SLAM-associated protein deficiency;XIAP deficiency;X-linked inhibitor of apoptosis deficiency;Autoimmune lymphoproliferative syndrome;ALPS;Other diseases of immune dysregulation;Familial hemophagocytic syndrome;FHPS;Familial hemophagocytic lymphohistiocytosis;FHL;Perforin deficiency;Munc13-4 deficiency;Syntaxin 11 deficiency;Munc18-2 deficiency;Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy;APECED;Autoimmune polyglandular syndrome;APS;Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome;IPEX syndrome;CD25 deficiency;ITCH deficiency;Severe congenital neutropenia;Cyclic neutropenia;Other congenital defects of neutrophil function;p14 deficiency;Glycogen storage disease type Ib;Leukocyte adhesion deficiency;Shwachman-Diamond syndrome;Chronic granulomatous disease;Myeloperoxidase deficiency;Mendelian susceptibility to mycobacterial disease;MSMD;Other congenital defects of phagocyte function;Anhidrotic ectodermal dysplasia with immunodeficiency;EDA-ID;Interleukin-1 receptor-associated kinase-4 deficiency;IRAK4 deficiency;MyD88 deficiency;Chronic mucocutaneous candidiasis;Other defects in innate immunity;Warts, hypogammaglobulinemia, infections, myelokathexis syndrome;WHIM syndrome;Congenital complement deficiency;C1q deficiency;C1r deficiency;C1s deficiency;C2 deficiency;C3 deficiency;C4 deficiency;C5 deficiency;C6 deficiency;C7 deficiency;C8 deficiency;C9 deficiency;Hereditary angioedema;C1 inhibitor deficiency;Inherited deficiency of complement system;Factor D deficiency;Factor I deficiency;Factor H deficiency;Properdin deficiency;MASP1 deficiency;MASP2 deficiency;3MC syndrome;Immunodeficiency associated with FCN3 mutation;FCN3; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
122	Peroxisome 💬	[1] XDH 💬 Peroxisome × Name Full Name XDH xanthine dehydrogenase	Allopurinol 💬 Peroxisome × Name Other Names Allopurinol Allopurinol (JP18/USP/INN) Zyloprim (TN) ALLOPURINOL	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 122. Peroxisome × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
123	Peroxisome 💬	[1] XDH 💬 Peroxisome × Name Full Name XDH xanthine dehydrogenase	Allopurinol sodium 💬 Peroxisome × Name Other Names Allopurinol sodium Allopurinol sodium Aloprim (TN) ALOPRIM ALLOPURINOL ALLOPURINOL SODIUM	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 122. Peroxisome × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
124	Phospholipase D signaling pathway 💬	[1] AGTR1 💬 Phospholipase D signaling pathway × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Phospholipase D signaling pathway × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 124. Phospholipase D signaling pathway × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
125	PI3K-Akt signaling pathway 💬	[1] CSF3R 💬 PI3K-Akt signaling pathway × Name Full Name CSF3R colony stimulating factor 3 receptor	Lenograstim 💬 PI3K-Akt signaling pathway × Name Other Names Lenograstim Lenograstim (USAN/INN) Lenograstim (genetical recombination) (JP18) Neutrogin (TN)	Lenograstim	[8]  2 , 13, 16, 18, 19, 57, 65, 97 💬 125. PI3K-Akt signaling pathway × Disease ID Name  2  Amyotrophic lateral sclerosis;ALS; 13 Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis; 16 Crow-Fukase syndrome;Polyneuropathy, organomegaly, endocrinopathy, m-protein, and skin changes syndrome;POEMS syndrome;Takatsuki disease;Polyneuropathy, endocrinopathy, plasma cell dyscrasia syndrome;PEP syndrome; 18 Spinocerebellar degeneration;SCD;:Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysial atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;Neu:Ataxia with vitamin E deficiency;AVED;Aprataxin deficiency;APTX deficiency;Friedreich ataxia;FRDA;Senataxin deficiency;SETX deficiency;Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Spastic ataxia; 19 Lysosomal storage disease;Lysosomal disease;Gaucher disease;Niemann-Pick disease type A/B;Niemann-Pick type A;NPD-A;NPA;Niemann-Pick type B;NPD-B;NPB;Acid sphingomyelinase deficiency;ASMD;Niemann-Pick disease type C;Niemann-Pick type C;NPD-C;NPC;GM1-gangliosidosis;GM1-gangliosidoses;GM2-gangliosidosis;GM2-gangliosidoses;Tay-Sachs disease;Sandhoff disease;Krabbe disease;Metachromatic leukodystrophy;MLD;Multiple-sulfatase deficiency;Farber disease;Mucopolysaccharidosis type I;Mucopolysaccharidosis I;MPS I;Hurler syndrome;Hurler-Scheie syndrome;Scheie syndrome;Mucopolysaccharidosis type II;Mucopolysaccharidosis II;MPS II;Hunter syndrome;Mucopolysaccharidosis type III;Mucopolysaccharidosis III;MPS III;Sanfilippo syndrome;Mucopolysaccharidosis type IV;Mucopolysaccharidosis IV;MPS IV;MPS IVA;Morquio syndrome;Morquio A syndrome;Mucopolysaccharidosis type VI;Mucopolysaccharidosis VI;MPS VI;Maroteaux-Lamy syndrome;Mucopolysaccharidosis type VII;Mucopolysaccharidosis VII;MPS VII;Sly syndrome;Mucopolysaccharidosis type IX;Mucopolysaccharidosis IX;MPS IX;Hyaluronidase deficiency;Sialidosis;Galactosialidosis;Mucolipidosis II;Mucolipidosis type II;I-cell disease;Mucolipidosis III;Mucolipidosis type III;Alpha-Mannosidosis;Alpha-Mannosidase Deficiency;Beta-Mannosidosis;Beta-Mannosidase Deficiency;Fucosidosis;Aspartylglucosaminuria;Schindler disease;Kanzaki disease;Pompe disease;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Ceroid lipofuscinosis;Fabry disease;Cystinosis; 57 Idiopathic dilated cardiomyopathy; 65 Primary immunodeficiency;X-linked severe combined immunodeficiency;X-SCID;Reticular dysgenesis;Adenosine deaminase deficiency;Omenn syndrome;Purine nucleoside phosphorylase deficiency;CD8 deficiency;ZAP-70 deficiency;MHC class I deficiency;MHC class II deficiency;Other combined immunodeficiencies;Wiskott-Aldrich syndrome;WAS;Ataxia telangiectasia;Nijmegen breakage syndrome;Bloom syndrome;Immunodeficiency, centromere region instability, facial anomalies syndrome;ICF syndrome;PMS2 deficiency;Radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties syndrome;RIDDLE syndrome;Schimke syndrome;Netherton syndrome;Thymic hypoplasia;DiGeorge syndrome;22q11.2 deletion syndrome;Hyper-IgE syndrome;Hepatic venoocclusive immunodeficiency;Immunodeficiency with central hepatic vein atresia;Dyskeratosis congenita;X-linked agammaglobulinaemia;Common variable immunodeficiency;Hyper-IgM syndrome;Isolated IgG subclass deficiency;Selective IgA deficiency;Specific antibody production deficiency;Infant transient hypogammaglobulinemia;Other predominantly antibody deficiencies;Chédiak-Higashi syndrome;Chediak-Higashi syndrome;X-linked lymphoproliferative syndrome;SAP deficiency;SH2D1A/SLAM-associated protein deficiency;XIAP deficiency;X-linked inhibitor of apoptosis deficiency;Autoimmune lymphoproliferative syndrome;ALPS;Other diseases of immune dysregulation;Familial hemophagocytic syndrome;FHPS;Familial hemophagocytic lymphohistiocytosis;FHL;Perforin deficiency;Munc13-4 deficiency;Syntaxin 11 deficiency;Munc18-2 deficiency;Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy;APECED;Autoimmune polyglandular syndrome;APS;Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome;IPEX syndrome;CD25 deficiency;ITCH deficiency;Severe congenital neutropenia;Cyclic neutropenia;Other congenital defects of neutrophil function;p14 deficiency;Glycogen storage disease type Ib;Leukocyte adhesion deficiency;Shwachman-Diamond syndrome;Chronic granulomatous disease;Myeloperoxidase deficiency;Mendelian susceptibility to mycobacterial disease;MSMD;Other congenital defects of phagocyte function;Anhidrotic ectodermal dysplasia with immunodeficiency;EDA-ID;Interleukin-1 receptor-associated kinase-4 deficiency;IRAK4 deficiency;MyD88 deficiency;Chronic mucocutaneous candidiasis;Other defects in innate immunity;Warts, hypogammaglobulinemia, infections, myelokathexis syndrome;WHIM syndrome;Congenital complement deficiency;C1q deficiency;C1r deficiency;C1s deficiency;C2 deficiency;C3 deficiency;C4 deficiency;C5 deficiency;C6 deficiency;C7 deficiency;C8 deficiency;C9 deficiency;Hereditary angioedema;C1 inhibitor deficiency;Inherited deficiency of complement system;Factor D deficiency;Factor I deficiency;Factor H deficiency;Properdin deficiency;MASP1 deficiency;MASP2 deficiency;3MC syndrome;Immunodeficiency associated with FCN3 mutation;FCN3; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
126	Purine metabolism 💬	[1] XDH 💬 Purine metabolism × Name Full Name XDH xanthine dehydrogenase	Allopurinol 💬 Purine metabolism × Name Other Names Allopurinol Allopurinol (JP18/USP/INN) Zyloprim (TN) ALLOPURINOL	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 126. Purine metabolism × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
127	Purine metabolism 💬	[1] XDH 💬 Purine metabolism × Name Full Name XDH xanthine dehydrogenase	Allopurinol sodium 💬 Purine metabolism × Name Other Names Allopurinol sodium Allopurinol sodium Aloprim (TN) ALOPRIM ALLOPURINOL ALLOPURINOL SODIUM	Allopurinol	[7]  6 , 46, 57, 60, 66, 96, 97 💬 126. Purine metabolism × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 60 Aplastic anemia; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 96 Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD; 97 Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
128	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Regulation of lipolysis in adipocytes × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 128. Regulation of lipolysis in adipocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
129	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Regulation of lipolysis in adipocytes × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 128. Regulation of lipolysis in adipocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
130	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Regulation of lipolysis in adipocytes × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 128. Regulation of lipolysis in adipocytes × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
131	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Regulation of lipolysis in adipocytes × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 131. Regulation of lipolysis in adipocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
132	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Regulation of lipolysis in adipocytes × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 131. Regulation of lipolysis in adipocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
133	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Regulation of lipolysis in adipocytes × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 131. Regulation of lipolysis in adipocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
134	Regulation of lipolysis in adipocytes 💬	[1] ADRB1 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Regulation of lipolysis in adipocytes × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 131. Regulation of lipolysis in adipocytes × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
135	Regulation of lipolysis in adipocytes 💬	[2] ADRB1, ADRB2 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Regulation of lipolysis in adipocytes × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 135. Regulation of lipolysis in adipocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
136	Regulation of lipolysis in adipocytes 💬	[2] ADRB1, ADRB2 💬 Regulation of lipolysis in adipocytes × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Regulation of lipolysis in adipocytes × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 135. Regulation of lipolysis in adipocytes × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
137	Renin secretion 💬	[1] ACE 💬 Renin secretion × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Renin secretion × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 137. Renin secretion × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
138	Renin secretion 💬	[1] ACE 💬 Renin secretion × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Renin secretion × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 137. Renin secretion × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
139	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Renin secretion × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 139. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
140	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Renin secretion × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 139. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
141	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Renin secretion × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 139. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
142	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Renin secretion × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 142. Renin secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
143	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Renin secretion × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 142. Renin secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
144	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Renin secretion × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 142. Renin secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
145	Renin secretion 💬	[1] ADRB1 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Renin secretion × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 142. Renin secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
146	Renin secretion 💬	[2] ADRB1, ADRB2 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Renin secretion × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 146. Renin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
147	Renin secretion 💬	[2] ADRB1, ADRB2 💬 Renin secretion × Name Full Name ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Renin secretion × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 146. Renin secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
148	Renin secretion 💬	[1] AGTR1 💬 Renin secretion × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Renin secretion × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 148. Renin secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
149	Renin-angiotensin system 💬	[1] ACE 💬 Renin-angiotensin system × Name Full Name ACE angiotensin I converting enzyme	Benazepril hydrochloride 💬 Renin-angiotensin system × Name Other Names Benazepril hydrochloride Benazepril hydrochloride (JAN/USP) Lotensin (TN)	Benazepril	[4] 49, 57, 218, 224 💬 149. Renin-angiotensin system × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
150	Renin-angiotensin system 💬	[1] ACE 💬 Renin-angiotensin system × Name Full Name ACE angiotensin I converting enzyme	Benazepril 💬 Renin-angiotensin system × Name Other Names Benazepril Benazepril (INN) Benazepril Sandoz (TN) Forteekor [veterinary] (TN)	Benazepril	[4] 49, 57, 218, 224 💬 149. Renin-angiotensin system × Disease ID Name 49 Systemic lupus erythematosus;SLE; 57 Idiopathic dilated cardiomyopathy; 218 Alport syndrome; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
151	Renin-angiotensin system 💬	[1] AGTR1 💬 Renin-angiotensin system × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Renin-angiotensin system × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 151. Renin-angiotensin system × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;
152	Salivary secretion 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Salivary secretion × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol 💬 Salivary secretion × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 152. Salivary secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
153	Salivary secretion 💬	[5] ADRA1A, ADRA1B, ADRA1D, ADRB1, ADRB2 💬 Salivary secretion × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D ADRB1 adrenoceptor beta 1 ADRB2 adrenoceptor beta 2	Carvedilol phosphate 💬 Salivary secretion × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 152. Salivary secretion × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
154	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine hydrochloride 💬 Salivary secretion × Name Other Names Dobutamine hydrochloride Dobutamine hydrochloride (JP18/USP) Dobutrex (TN) DOBUTAMINE DOBUTAMINE HYDROCHLORIDE DOBUTAMINE HYDROCHLORIDE IN DEXTROSE DOBUTAMINE IN DEXTROSE	Dobutamine	[4] 57, 58, 86, 215 💬 154. Salivary secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
155	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine 💬 Salivary secretion × Name Other Names Dobutamine Dobutamine (USAN/INN)	Dobutamine	[4] 57, 58, 86, 215 💬 154. Salivary secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
156	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Dobutamine tartrate 💬 Salivary secretion × Name Other Names Dobutamine tartrate Dobutamine tartrate (USAN)	Dobutamine	[4] 57, 58, 86, 215 💬 154. Salivary secretion × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 86 Pulmonary arterial hypertension;PAH; 215 Tetralogy of Fallot;Fallot tetralogy;
157	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol tartrate 💬 Salivary secretion × Name Other Names Metoprolol tartrate Metoprolol tartrate (JP18/USP) Lopressor (TN) LOPRESSOR METOPROLOL METOPROLOL TARTRATE	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 157. Salivary secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
158	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol succinate 💬 Salivary secretion × Name Other Names Metoprolol succinate Metoprolol succinate (USP) Toprol XL (TN) KAPSPARGO METOPROLOL SUCCINATE TOPROL TOPROL XL METOPROLOL SUCCINATE ER	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 157. Salivary secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
159	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol 💬 Salivary secretion × Name Other Names Metoprolol Metoprolol (USAN/INN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 157. Salivary secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
160	Salivary secretion 💬	[1] ADRB1 💬 Salivary secretion × Name Full Name ADRB1 adrenoceptor beta 1	Metoprolol fumarate 💬 Salivary secretion × Name Other Names Metoprolol fumarate Metoprolol fumarate (USP) Lopressor (TN)	Metoprolol	[6] 17, 57, 58, 113, 193, 226 💬 157. Salivary secretion × Disease ID Name 17 Multiple system atrophy;MSA;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome; 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 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;Muscle-eye-brain 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; 193 Prader-Willi syndrome; 226 Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
161	Vascular smooth muscle contraction 💬	[3] ADRA1A, ADRA1B, ADRA1D 💬 Vascular smooth muscle contraction × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D	Carvedilol 💬 Vascular smooth muscle contraction × Name Other Names Carvedilol Carvedilol (JP18/USP/INN) Artist (TN) Coreg (TN) COREG CARVEDILOL	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 161. Vascular smooth muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
162	Vascular smooth muscle contraction 💬	[3] ADRA1A, ADRA1B, ADRA1D 💬 Vascular smooth muscle contraction × Name Full Name ADRA1A adrenoceptor alpha 1A ADRA1B adrenoceptor alpha 1B ADRA1D adrenoceptor alpha 1D	Carvedilol phosphate 💬 Vascular smooth muscle contraction × Name Other Names Carvedilol phosphate Carvedilol phosphate (USAN) Carvedilol phosphate hydrate (JAN) Coreg CR (TN) COREG CR CARVEDILOL PHOSPHATE	Carvedilol	[6]  6 , 46, 57, 86, 113, 210 💬 161. Vascular smooth muscle contraction × Disease ID Name  6  Parkinson disease;Disease Parkinson's; 46 Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV; 57 Idiopathic dilated cardiomyopathy; 86 Pulmonary arterial hypertension;PAH; 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;Muscle-eye-brain 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; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome;
163	Vascular smooth muscle contraction 💬	[1] AGTR1 💬 Vascular smooth muscle contraction × Name Full Name AGTR1 angiotensin II receptor type 1	Valsartan 💬 Vascular smooth muscle contraction × Name Other Names Valsartan Valsartan (JP18/USP/INN) Diovan (TN) DIOVAN VALSARTAN	Valsartan	[8] 57, 58, 66, 75, 86, 210, 222, 224 💬 163. Vascular smooth muscle contraction × Disease ID Name 57 Idiopathic dilated cardiomyopathy; 58 Hypertrophic cardiomyopathy;HCM; 66 IgA nephropathy;IgA nephritis;Berger disease;IgA-IgG nephropathy; 75 Cushing disease;Cushing syndrome; 86 Pulmonary arterial hypertension;PAH; 210 Single Ventricle;SV;Single ventricle heart defect;Univentricular heart;UVH;Single ventricular circulation syndrome; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN; 224 Purpura nephritis;Henoch-Schönlein purpura nephritis;HSPN;

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