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
Displaying entries 14051 - 14075 of 62743 in total
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