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 |
---|---|---|---|---|---|
C0795907 | CONOTRUNCAL ANOMALY FACE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0020626 | Hypoparathyroidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C3160718 | PARKINSON DISEASE, LATE-ONSET | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0010054 | Coronary Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0026269 | Mitral Valve Stenosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0032914 | Pre-Eclampsia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
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 |
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Last updated: August 19, 2024