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KEGG PATHWAY
On map,
Yellow:
Drug target,
Red:
All disease-related
KEGG GENES
KEGG DRUG
DrugBank
Disease ID
1
Circadian rhythm
💬
2 genes, 1 drug (DrugBank) and 25 diseases
PRKAA1
[2]
PRKAA1
,
PRKAA2
💬
Circadian rhythm
×
Name
Full Name
PRKAA1
protein kinase AMP-activated catalytic subunit alpha 1
PRKAA2
protein kinase AMP-activated catalytic subunit alpha 2
Metformin
Metformin
💬
Circadian rhythm
×
Name
Other Names
Metformin
Metformin (USAN/INN)
Metformin
002
[25]
2
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6
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8
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13
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46
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49
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60
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65
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67
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75
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77
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81
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86
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97
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113
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127
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158
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206
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218
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225
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233
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265
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285
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299
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301
💬
[25]
2
,
6
,
8
,
13
,
46
,
49
,
60
,
65
,
67
,
75
,
77
,
81
,
86
,
97
,
113
,
127
,
158
,
206
,
218
,
225
,
233
,
2
...
1.
Circadian rhythm
×
Disease ID
Name
2
Amyotrophic lateral sclerosis;ALS;
6
Parkinson disease;Disease Parkinson's;
8
Huntington disease;Huntington chorea;
13
Multiple sclerosis/Neuromyelitis optica;
46
Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;
49
Systemic lupus erythematosus;SLE;
60
Aplastic anemia;
65
Primary immunodeficiency;
67
Polycystic kidney disease;PKD;PCKD;Polycystic kidney;
75
Cushing disease;Cushing;
77
Growth hormone secreting pituitary adenoma;Pituitary growth hormone secretion hyperthyroidism;
81
Congenital adrenal hyperplasia;CAH;Congenital adrenal enzyme deficiency;Congenial adrenal cortex enzyme deficiency;
86
Pulmonary arterial hypertension;PAH;
97
Ulcerative colitis;
113
Muscular dystrophy;
127
Frontotemporal lobar degeneration;
158
Tuberous sclerosis;Tuberous sclerosis complex;
206
Fragile X syndrome;
218
Alport syndrome;
225
Congenital nephrogenic diabetes insipidus;Hereditary nephrogenic diabetes insipidus;Nephrogenic diabetes insipidus;
233
Wolfram syndrome;Diabetes Insipidus, Diabetes mellitus, optic atrophy, and deafness syndrome;DIDMOAD syndrome;
265
Lipodystrophy;
285
Fanconi anemia;
299
Cystic fibrosis;
301
Macular dystrophy;