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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0751571 | Cancer of Urinary Tract | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0266295 | Congenital hypoplasia of kidney | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0042571 | Vertigo | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0917799 | Hypersomnia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0600241 | heroin abuse | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020179 | Huntington Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0007137 | Squamous cell carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1333990 | Hereditary Nonpolyposis Colorectal Cancer | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0011573 | Endogenous depression | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0027932 | Neurotic Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0001418 | Adenocarcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020224 | Polyhydramnios | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1336076 | Sporadic Breast Carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0042487 | Venous Thrombosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0021151 | Incipient Schizophrenia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0085159 | Seasonal Affective Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1847360 | PARKINSON DISEASE 10 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0403447 | Chronic Kidney Insufficiency | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004096 | Asthma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020550 | Hyperthyroidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0019196 | Hepatitis C | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C2750737 | DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0751039 | Cockayne Syndrome, Type I | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C3888239 | HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0238378 | Desquamative interstitial pneumonia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
