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Gene

Search results

No.

KEGG PATHWAY
On map, Yellow: Drug target, Red: All disease-related

GABAergic synapse 💬

[1] ABAT 💬

Vigabatrin 💬

Vigabatrin

[2] 145, 158 💬

Disease ID	Name
145	West syndrome;Infantile spasm;Infantile spasms;Infantile spasms syndrome;Infantile epileptic spasms;Infantile epileptic spasms syndrome;
158	Tuberous sclerosis;Tuberous sclerosis complex;TSC;

GABAergic synapse 💬

[3] ABAT, GAD1, GAD2 💬

Divalproex sodium 💬

Valproic acid

[11] 3 , 5 , 26, 34, 51, 65, 89, 90, 145, 222, 331 💬

Disease ID	Name
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
5	Progressive supranuclear palsy;PSP;
26	HTLV-1-associated myelopathy;Tropical spastic paraparesis;HTLV-1;HTLV-I;HAM;
34	Neurofibromatosis;Neurofibromatosis type 1;NF1;Recklinghausen disease;Neurofibromatosis type 2;NF2;
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
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;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;
89	Lymphangioleiomyomatosis;LAM;
90	Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
145	West syndrome;Infantile spasm;Infantile spasms;Infantile spasms syndrome;Infantile epileptic spasms;Infantile epileptic spasms syndrome;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
331	Idiopathic multicentric castleman disease;iMCD;Castleman disease;

GABAergic synapse 💬

[3] ABAT, GAD1, GAD2 💬

Valproic acid 💬

Valproic acid

[11] 3 , 5 , 26, 34, 51, 65, 89, 90, 145, 222, 331 💬

Disease ID	Name
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
5	Progressive supranuclear palsy;PSP;
26	HTLV-1-associated myelopathy;Tropical spastic paraparesis;HTLV-1;HTLV-I;HAM;
34	Neurofibromatosis;Neurofibromatosis type 1;NF1;Recklinghausen disease;Neurofibromatosis type 2;NF2;
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
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;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;
89	Lymphangioleiomyomatosis;LAM;
90	Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
145	West syndrome;Infantile spasm;Infantile spasms;Infantile spasms syndrome;Infantile epileptic spasms;Infantile epileptic spasms syndrome;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
331	Idiopathic multicentric castleman disease;iMCD;Castleman disease;

GABAergic synapse 💬

[3] ABAT, GAD1, GAD2 💬

Valproate sodium 💬

Valproic acid

[11] 3 , 5 , 26, 34, 51, 65, 89, 90, 145, 222, 331 💬

Disease ID	Name
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
5	Progressive supranuclear palsy;PSP;
26	HTLV-1-associated myelopathy;Tropical spastic paraparesis;HTLV-1;HTLV-I;HAM;
34	Neurofibromatosis;Neurofibromatosis type 1;NF1;Recklinghausen disease;Neurofibromatosis type 2;NF2;
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
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;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;
89	Lymphangioleiomyomatosis;LAM;
90	Retinitis pigmentosa;Rod dystrophy;Cone-rod dystrophy;Rod-Cone Dystrophy;
145	West syndrome;Infantile spasm;Infantile spasms;Infantile spasms syndrome;Infantile epileptic spasms;Infantile epileptic spasms syndrome;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
331	Idiopathic multicentric castleman disease;iMCD;Castleman disease;

GABAergic synapse 💬

[5] CACNA1B, CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1B	voltage-dependent N-type calcium channel subunit alpha-1B isoform 1
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Cilnidipine 💬

Cilnidipine

[1] 67 💬

Disease ID	Name
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Amlodipine besylate 💬

Amlodipine

[6] 51, 67, 79, 113, 222, 298 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
79	Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia;
113	Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Amlodipine maleate 💬

Amlodipine

[6] 51, 67, 79, 113, 222, 298 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
79	Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia;
113	Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Amlodipine 💬

Amlodipine

[6] 51, 67, 79, 113, 222, 298 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
79	Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia;
113	Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Amlodipine benzoate 💬

Amlodipine

[6] 51, 67, 79, 113, 222, 298 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
79	Homozygous familial hypercholesterolemia;Familial hypercholesterolemia;Familial hypercholesterolaemia;
113	Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;WWS;Muscle-Eye-Brain disease;MEB disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy;
222	Primary nephrotic syndrome;Nephrotic syndrome;Glomerulonephritis;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Crescentic glomerulonephritis;CGN;CrGN;Endocapillary proliferative glomerulonephritis;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Benidipine hydrochloride 💬

Benidipine

[1] 57 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Benidipine 💬

Benidipine

[1] 57 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Bevantolol hydrochloride 💬

Bevantolol

[1] 8 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Diltiazem hydrochloride 💬

Name	Other Names
Diltiazem hydrochloride	Cardizem Cartia XT Dilacor XR Dilt-CD CARDIZEM CD CARDIZEM LA DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE TIAZAC CARTIA DILTIAZEM HCI DILTIAZEM HCL ER DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE MATZIM LA TIADYLT ER

Diltiazem

[4] 51, 58, 86, 88 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
58	Hypertrophic cardiomyopathy;HCM;
86	Pulmonary arterial hypertension;PAH;
88	Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Diltiazem malate 💬

Diltiazem

[4] 51, 58, 86, 88 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
58	Hypertrophic cardiomyopathy;HCM;
86	Pulmonary arterial hypertension;PAH;
88	Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Diltiazem 💬

Diltiazem

[4] 51, 58, 86, 88 💬

Disease ID	Name
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
58	Hypertrophic cardiomyopathy;HCM;
86	Pulmonary arterial hypertension;PAH;
88	Chronic thromboembolic pulmonary hypertension;CTEPH;Idiopathic chronic pulmonary thromboembolism;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Isradipine 💬

Isradipine

[1] 6 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Nicardipine hydrochloride 💬

Nicardipine

[2] 70, 86 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Nicardipine 💬

Nicardipine

[2] 70, 86 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Nifedipine 💬

Nifedipine

[2] 50, 81 💬

Disease ID	Name
50	Dermatomyositis;Polymyositis;Idiopathic inflammatory myositis;IIM;
81	Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;Aldosterone synthase deficiency;Congenital Lipoid Adrenal Hyperplasia;3β-Hydroxysteroid Dehydrogenase Deficiency;21-Hydroxylase deficiency;21-OHD;11β-Hydroxylase deficiency;17α-Hydroxylase deficiency;P450 oxidoreductase deficiency;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Nilvadipine 💬

Nilvadipine

[1] 90 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Perhexiline maleate 💬

Perhexiline

[2] 58, 272 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Perhexiline 💬

Perhexiline

[2] 58, 272 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Propiverine hydrochloride 💬

Propiverine

[1] 226 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Propiverine 💬

Propiverine

[1] 226 💬

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Verapamil hydrochloride 💬

Verapamil

[5] 57, 58, 96, 140, 167 💬

Disease ID	Name
57	Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
58	Hypertrophic cardiomyopathy;HCM;
96	Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD;
140	Dorabe syndrome;Dravet syndrome;
167	Marfan syndrome;Loeys-Dietz syndrome;LDS;

GABAergic synapse 💬

[4] CACNA1C, CACNA1D, CACNA1F, CACNA1S 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S

Verapamil 💬

Verapamil

[5] 57, 58, 96, 140, 167 💬

Disease ID	Name
57	Idiopathic dilated cardiomyopathy;Dilated cardiomyopathy;DCM;
58	Hypertrophic cardiomyopathy;HCM;
96	Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD;
140	Dorabe syndrome;Dravet syndrome;
167	Marfan syndrome;Loeys-Dietz syndrome;LDS;

GABAergic synapse 💬

[20] CACNA1C, CACNA1D, CACNA1F, CACNA1S, GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
CACNA1C	voltage-dependent L-type calcium channel subunit alpha-1C isoform 18
CACNA1D	voltage-dependent L-type calcium channel subunit alpha-1D isoform b
CACNA1F	voltage-dependent L-type calcium channel subunit alpha-1F isoform 1
CACNA1S	voltage-dependent L-type calcium channel subunit alpha-1S
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Topiramate 💬

Topiramate

[6] 6 , 97, 140, 144, 156, 193 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
140	Dorabe syndrome;Dravet syndrome;
144	Lennox-Gastaut syndrome;
156	Rett syndrome;
193	Prader-Willi syndrome;

GABAergic synapse 💬

[1] CACNA1S 💬

Pinaverium bromide 💬

Pinaverium

[1] 298 💬

GABAergic synapse 💬

[2] GABBR1, GABBR2 💬

Arbaclofen 💬

Arbaclofen

[2] 13, 206 💬

Disease ID	Name
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
206	Fragile X syndrome;

GABAergic synapse 💬

[2] GABBR1, GABBR2 💬

Arbaclofen placarbil 💬

Arbaclofen Placarbil

[1] 13 💬

GABAergic synapse 💬

[2] GABBR1, GABBR2 💬

Baclofen 💬

Baclofen

[8] 2 , 10, 13, 18, 65, 70, 149, 206 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
10	Charcot-Marie-Tooth disease;CMT;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
18	Spinocerebellar degeneration;SCD;Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysian atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;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;
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;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;
70	Spinal stenosis;Extensive spinal canal stenosis;
149	Hemiconvulsion hemiplegia epilepsy syndrome;One side convulsions;Hemiplegia;Epilepsy syndrome;
206	Fragile X syndrome;

GABAergic synapse 💬

[1] GABRA1 💬

Etomidate 💬

Etomidate

[2] 6 , 11 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Alprazolam 💬

Alprazolam

[2] 8 , 75 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Clobazam 💬

Clobazam

[2] 140, 144 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Clonazepam 💬

Clonazepam

[1] 6 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Diazepam 💬

Diazepam

[3] 46, 155, 298 💬

Disease ID	Name
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;
155	Acquired aphasia with convulsive disorder;Landau-Kleffner syndrome;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Eszopiclone 💬

Eszopiclone

[3] 6 , 13, 46 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Flumazenil 💬

Flumazenil

[5] 6 , 13, 17, 18, 206 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
17	Multiple system atrophy;MSA;Olivopontocerebellar atrophy;OPCA;Striatonigral degeneration;Shy-Drager syndrome;
18	Spinocerebellar degeneration;SCD;Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysian atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;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;
206	Fragile X syndrome;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Fospropofol disodium 💬

Fospropofol

[1] 226 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Gaboxadol 💬

Gaboxadol

[2] 201, 206 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Ganaxolone 💬

Ganaxolone

[4] 145, 152, 158, 206 💬

Disease ID	Name
145	West syndrome;Infantile spasm;Infantile spasms;Infantile spasms syndrome;Infantile epileptic spasms;Infantile epileptic spasms syndrome;
152	PCDH19-related syndrome;PCDH19-related epilepsy syndrome;PCDH19 Epilepsy;Epilepsy and mental retardation limited to females;PCDH19 female pediatric epilepsy;PCDH19 related epilepsy;Protocadherin 19 (PCDH19)-related epilepsy;
158	Tuberous sclerosis;Tuberous sclerosis complex;TSC;
206	Fragile X syndrome;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Lorazepam 💬

Lorazepam

[2] 36, 231 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Midazolam 💬

Midazolam

[14] 2 , 3 , 6 , 13, 21, 46, 67, 70, 96, 97, 231, 272, 298, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
21	Mitochondrial disease;Choronic progressive external ophthalmolegia;CPEO;Leigh syndrome;Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode;MELAS;Myoclonus epilepsy associated with ragged-red fibers;MERRF;Mitochondrial respiratory chain disorders;Pearson syndrome;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
70	Spinal stenosis;Extensive spinal canal stenosis;
96	Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
231	Alpha-1-antitrypsin deficiency;AATD;
272	Fibrodysplasia ossificans progressiva;FOP;
298	Hereditary pancreatitis;Chronic pancreatitis;
299	Cystic fibrosis;CF;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Midazolam hydrochloride 💬

Midazolam

[14] 2 , 3 , 6 , 13, 21, 46, 67, 70, 96, 97, 231, 272, 298, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
21	Mitochondrial disease;Choronic progressive external ophthalmolegia;CPEO;Leigh syndrome;Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode;MELAS;Myoclonus epilepsy associated with ragged-red fibers;MERRF;Mitochondrial respiratory chain disorders;Pearson syndrome;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
70	Spinal stenosis;Extensive spinal canal stenosis;
96	Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
231	Alpha-1-antitrypsin deficiency;AATD;
272	Fibrodysplasia ossificans progressiva;FOP;
298	Hereditary pancreatitis;Chronic pancreatitis;
299	Cystic fibrosis;CF;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Midazolam maleate 💬

Midazolam

[14] 2 , 3 , 6 , 13, 21, 46, 67, 70, 96, 97, 231, 272, 298, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
21	Mitochondrial disease;Choronic progressive external ophthalmolegia;CPEO;Leigh syndrome;Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode;MELAS;Myoclonus epilepsy associated with ragged-red fibers;MERRF;Mitochondrial respiratory chain disorders;Pearson syndrome;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;
70	Spinal stenosis;Extensive spinal canal stenosis;
96	Crohn disease;CD;Terminal ileitis;Inflammatory bowel disease;IBD;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
231	Alpha-1-antitrypsin deficiency;AATD;
272	Fibrodysplasia ossificans progressiva;FOP;
298	Hereditary pancreatitis;Chronic pancreatitis;
299	Cystic fibrosis;CF;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Nitrazepam 💬

Nitrazepam

[1] 145 💬

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Propofol 💬

Propofol

[10] 3 , 6 , 21, 22, 34, 46, 70, 97, 98, 296 💬

Disease ID	Name
3	Spinal muscular atrophy;SMA;Myelopathic muscular atrophy;Werdnig-Hoffman disease;Dubowitz disease;Kugelberg-Welander disease;Dubowitz syndrome;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
21	Mitochondrial disease;Choronic progressive external ophthalmolegia;CPEO;Leigh syndrome;Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode;MELAS;Myoclonus epilepsy associated with ragged-red fibers;MERRF;Mitochondrial respiratory chain disorders;Pearson syndrome;
22	Moyamoya disease;Occlusive disease in circle of Willis;
34	Neurofibromatosis;Neurofibromatosis type 1;NF1;Recklinghausen disease;Neurofibromatosis type 2;NF2;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;
70	Spinal stenosis;Extensive spinal canal stenosis;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;
98	Eosinophilic gastro-intestinal disorder;Eosinophilic gastrointestinal disorder;EGID;Eosinophilic gastrointestinal disease;Eosinophilic gastroenteritis;Eosinophilic esophagitis;Eosinophilic colitis;Neonatal food-protein induced enterocolitis syndrome;Neonatal food-protein induced enterocolitis;N-FPIES;Eosinophilic esophagitis;EoE;Eosinophilic gastroenteritis;EGE;
296	Biliary atresia;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Remimazolam besylate 💬

Remimazolam

[3] 6 , 22, 97 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
22	Moyamoya disease;Occlusive disease in circle of Willis;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Remimazolam 💬

Remimazolam

[3] 6 , 22, 97 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
22	Moyamoya disease;Occlusive disease in circle of Willis;
97	Ulcerative colitis;UC;Inflammatory bowel disease;IBD;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Zolpidem tartrate 💬

Zolpidem

[3] 5 , 6 , 46 💬

Disease ID	Name
5	Progressive supranuclear palsy;PSP;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Zolpidem 💬

Zolpidem

[3] 5 , 6 , 46 💬

Disease ID	Name
5	Progressive supranuclear palsy;PSP;
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;Systemic rheumatoid vasculitis;SRV;

GABAergic synapse 💬

[16] GABRA1, GABRA2, GABRA3, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRE, GABRG1, GABRG2, GABRG3, GABRP, GABRQ 💬

Name	Full Name
GABRA1	gamma-aminobutyric acid receptor subunit alpha-1 precursor
GABRA2	gamma-aminobutyric acid receptor subunit alpha-2 isoform a precursor
GABRA3	gamma-aminobutyric acid receptor subunit alpha-3 precursor
GABRA4	gamma-aminobutyric acid receptor subunit alpha-4 isoform 1 precursor
GABRA5	gamma-aminobutyric acid receptor subunit alpha-5 precursor
GABRA6	gamma-aminobutyric acid receptor subunit alpha-6 precursor
GABRB1	gamma-aminobutyric acid receptor subunit beta-1 precursor
GABRB2	gamma-aminobutyric acid receptor subunit beta-2 isoform 1 precursor
GABRB3	gamma-aminobutyric acid receptor subunit beta-3 isoform 1 precursor
GABRD	gamma-aminobutyric acid receptor subunit delta precursor
GABRE	gamma-aminobutyric acid receptor subunit epsilon precursor
GABRG1	gamma-aminobutyric acid receptor subunit gamma-1 precursor
GABRG2	gamma-aminobutyric acid receptor subunit gamma-2 isoform 1 precursor
GABRG3	gamma-aminobutyric acid receptor subunit gamma-3 isoform 1 precursor
GABRP	gamma-aminobutyric acid receptor subunit pi isoform 1 precursor
GABRQ	gamma-aminobutyric acid receptor subunit theta precursor

Zopiclone 💬

Zopiclone

[1] 6 💬

GABAergic synapse 💬

[1] GABRA5 💬

Alogabat 💬

Alogabat

[1] 201 💬

GABAergic synapse 💬

[1] PRKCB 💬

Enzastaurin hydrochloride 💬

Enzastaurin

[1] 168 💬

Disease ID

Name

168

Ehlers-Danlos syndrome;EDS;Classic EDS;Classical EDS;cEDS;Classical-like Ehlers-Danlos syndrome;Classical-like EDS;clEDS;Cardiac-valvular Ehlers-Danlos syndrome;cvEDS;Vascular Ehlers-Danlos syndrome;Vascular EDS;vEDS;Hypermobile Ehlers-Danlos syndrome;Hypermobile EDS;hEDS;Arthrochalasia Ehlers-Danlos syndrome;Arthrochalasia EDS;aEDS;Dermatosparaxis Ehlers-Danlos syndrome;Dermatosparaxis EDS;dEDS;Kyphoscoliosis Ehlers-Danlos syndrome;Kyphoscoliosis EDS;kEDS;Brittle cornea syndrome;BCS;Spondylodysplastic Ehlers-Danlos Syndrome;spEDS;Musculocontractural Ehlers-Danlos Syndrome;mEDS;D4ST1-deficient Ehlers-Danlos syndrome;Dermatan 4-0-sulfotransferase 1-deficient EDS;D4ST1-deficient EDS;DDEDS;Myopathic Ehlers-Danlos Syndrome;mEDS;Periodontal Ehlers-Danlos Syndrome;pEDS;

GABAergic synapse 💬

[1] PRKCB 💬

Enzastaurin 💬

Enzastaurin

[1] 168 💬

Disease ID

Name

168

GABAergic synapse 💬

[1] SLC6A1 💬

Gabapentin 💬

Gabapentin

[7] 6 , 13, 18, 19, 70, 226, 298 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;Parkinson syndrome;Parkinsonian syndrome;
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
18	Spinocerebellar degeneration;SCD;Spinocerebellar ataxia;SCA;Machado-Joseph disease;MJD;Dentatorubural pallidoluysian atrophy;Dentatorubropallidoluysian atrophy;DRPLA;Naito-Koyanagi disease;Early-onset ataxia with ocular motor ataxia and hypoalbuminemia;EAOH;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;Krabbe syndrome;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;Schindler syndrome;Kanzaki disease;Kanzaki syndrome;Pompe disease;Pompe syndrome;Acid lipase deficiency;Wolman disease;Cholesterol ester storage disease;Danon disease;Danon syndrome;Free sialic acid storage disease;Infantile sialic acid storage disease;ISSD;Salla disease;Salla syndrome;Ceroid lipofuscinosis;Fabry disease;Cystinosis;
70	Spinal stenosis;Extensive spinal canal stenosis;
226	Interstitial cystitis with Hunners ulcer;Interstitial cystitis;
298	Hereditary pancreatitis;Chronic pancreatitis;

GABAergic synapse 💬

[1] SRC 💬

Bosutinib 💬

Bosutinib

[2] 2 , 67 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;

GABAergic synapse 💬

[1] SRC 💬

Bosutinib hydrate 💬

Bosutinib

[2] 2 , 67 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis;ALS;
67	Polycystic kidney disease;PKD;PCKD;Polycystic kidney;Autosomal dominant polycystic kidney disease;Autosomal dominant PKD;ADPKD;Autosomal recessive polycystic kidney disease;Autosomal recessive PKD;ARPKD;

GABAergic synapse 💬

[1] SRC 💬

Dasatinib 💬

Dasatinib

[3] 13, 51, 85 💬

Disease ID	Name
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
85	Idiopathic interstitial pneumonia;IIPs;Idiopathic pulmonary fibrosis;IPF;Idiopathic non-specific interstitial pneumonia;Idiopathic NSIP;Respiratory bronchiolitis - associated interstitial lung disease;RB-ILD;Desquamative interstitial pneumonia;DIP;Cryptogenic organizing pneumonia;COP;Acute interstitial pneumonia;AIP;Idiopathic lymphocytic interstitial pneumonia;Idiopathic LIP;Idiopathic PPFE;

GABAergic synapse 💬

[1] SRC 💬

Dasatinib 💬

Dasatinib

[3] 13, 51, 85 💬

Disease ID	Name
13	Multiple sclerosis/Neuromyelitis optica;Multiple sclerosis;Neuromyelitis optica;Neuromyelitis optica spectrum disorder;NMOSD;Balo concentric sclerosis;Baló concentric sclerosis;
51	Scleroderma;Systemic sclerosis;SSc;Diffuse cutaneous SSc;dcSSc;Limited cutaneous SSc;lcSSc;
85	Idiopathic interstitial pneumonia;IIPs;Idiopathic pulmonary fibrosis;IPF;Idiopathic non-specific interstitial pneumonia;Idiopathic NSIP;Respiratory bronchiolitis - associated interstitial lung disease;RB-ILD;Desquamative interstitial pneumonia;DIP;Cryptogenic organizing pneumonia;COP;Acute interstitial pneumonia;AIP;Idiopathic lymphocytic interstitial pneumonia;Idiopathic LIP;Idiopathic PPFE;

GABAergic synapse 💬

[1] SRC 💬

Saracatinib 💬

Saracatinib

[3] 6 , 89, 272 💬