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 13926 - 13950 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0026769 Multiple Sclerosis COMT 1312 catechol-O-methyltransferase P21964
C0015674 Chronic Fatigue Syndrome COMT 1312 catechol-O-methyltransferase P21964
C0684249 Carcinoma of lung COMT 1312 catechol-O-methyltransferase P21964
C0231528 Myalgia COMT 1312 catechol-O-methyltransferase P21964
C0497327 Dementia COMT 1312 catechol-O-methyltransferase P21964
C0001973 Alcoholic Intoxication, Chronic COMT 1312 catechol-O-methyltransferase P21964
C0520680 Sleep Apnea, Central COMT 1312 catechol-O-methyltransferase P21964
C0009806 Constipation COMT 1312 catechol-O-methyltransferase P21964
C0432215 Progressive pseudorheumatoid dysplasia COMT 1312 catechol-O-methyltransferase P21964
C0029421 Osteochondritis Dissecans COMT 1312 catechol-O-methyltransferase P21964
C0600139 Prostate carcinoma COMT 1312 catechol-O-methyltransferase P21964
C0026010 Microphthalmos COMT 1312 catechol-O-methyltransferase P21964
C0027404 Narcolepsy COMT 1312 catechol-O-methyltransferase P21964
C0042580 Vesico-Ureteral Reflux COMT 1312 catechol-O-methyltransferase P21964
C0011206 Delirium COMT 1312 catechol-O-methyltransferase P21964
C0002895 Anemia, Sickle Cell COMT 1312 catechol-O-methyltransferase P21964
C0003125 Anorexia Nervosa COMT 1312 catechol-O-methyltransferase P21964
C0029227 Delirium, Dementia, Amnestic, Cognitive Disorders COMT 1312 catechol-O-methyltransferase P21964
C0007134 Renal Cell Carcinoma COMT 1312 catechol-O-methyltransferase P21964
C0038454 Cerebrovascular accident COMT 1312 catechol-O-methyltransferase P21964
C1332206 Adult Lymphoma COMT 1312 catechol-O-methyltransferase P21964
C0700613 Anxiety state COMT 1312 catechol-O-methyltransferase P21964
C0524851 Neurodegenerative Disorders COMT 1312 catechol-O-methyltransferase P21964
C0015934 Fetal Growth Retardation COMT 1312 catechol-O-methyltransferase P21964
C0699885 Carcinoma of bladder COMT 1312 catechol-O-methyltransferase P21964

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Last updated: August 19, 2024