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 57801 - 57825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
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
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

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Last updated: August 19, 2024