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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 |
|---|---|---|---|---|---|
| C1145628 | Autonomic nervous system disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1868682 | Paroxysmal kinesigenic choreoathetosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1851710 | LATERAL MENINGOCELE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0039685 | Tetralogy of Fallot | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1868684 | EAR, PATELLA, SHORT STATURE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0024305 | Lymphoma, Non-Hodgkin | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013395 | Dyspepsia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009375 | Colonic Neoplasms | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0235974 | Pancreatic carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0346647 | Malignant neoplasm of pancreas | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0043207 | Wolfram Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020598 | Hypocalcemia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0021364 | Male infertility | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0026618 | Dental Fluorosis, Acquired | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009171 | Cocaine Abuse | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0033860 | Psoriasis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009595 | Obsessive-Compulsive Personality | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C3714756 | Intellectual Disability | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004930 | Behavior Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0019294 | Hernia, Inguinal | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0021051 | Immunologic Deficiency Syndromes | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0027051 | Myocardial Infarction | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0025958 | Microcephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0033578 | Prostatic Neoplasms | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0029124 | Optic Atrophy | COMT | 1312 | catechol-O-methyltransferase | P21964 |
