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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 |
|---|---|---|---|---|---|
| C1168401 | Squamous cell carcinoma of the head and neck | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0034150 | Purpura | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0029408 | Degenerative polyarthritis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0014070 | Encephalomyelitis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0036508 | Seborrheic dermatitis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0018817 | Atrial Septal Defects | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0017168 | Gastroesophageal reflux disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1704272 | Benign Prostatic Hyperplasia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0038379 | Strabismus | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0677886 | Epithelial ovarian cancer | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1839839 | MAJOR AFFECTIVE DISORDER 2 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0024141 | Lupus Erythematosus, Systemic | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0014173 | Endometrial Hyperplasia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0012746 | Dissociative disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0027609 | Neonatal Abstinence Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0302592 | Cervix carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0003466 | Anus, Imperforate | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0338831 | Manic | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0086769 | Panic Attacks | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020546 | Hypertensive crisis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0042900 | Vitiligo | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0039621 | Tetany | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1145628 | Autonomic nervous system disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1868682 | Paroxysmal kinesigenic choreoathetosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
