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 44801 - 44825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0020676 Hypothyroidism COMT 1312 catechol-O-methyltransferase P21964
C0085109 Corneal Neovascularization COMT 1312 catechol-O-methyltransferase P21964
C1862389 ATRIAL SEPTAL DEFECT 1 COMT 1312 catechol-O-methyltransferase P21964
C0036349 Paranoid Schizophrenia COMT 1312 catechol-O-methyltransferase P21964
C0012734 Disruptive Behavior Disorder COMT 1312 catechol-O-methyltransferase P21964
C0699790 Colon Carcinoma COMT 1312 catechol-O-methyltransferase P21964
C0338480 Common Migraine COMT 1312 catechol-O-methyltransferase P21964
C0036572 Seizures COMT 1312 catechol-O-methyltransferase P21964
C0025322 Premature Menopause COMT 1312 catechol-O-methyltransferase P21964
C0002902 Anencephaly COMT 1312 catechol-O-methyltransferase P21964
C0432306 Ichthyosis Bullosa of Siemens COMT 1312 catechol-O-methyltransferase P21964
C0007847 Malignant tumor of cervix COMT 1312 catechol-O-methyltransferase P21964
C0271441 Chronic otitis media COMT 1312 catechol-O-methyltransferase P21964
C1561643 Chronic Kidney Diseases COMT 1312 catechol-O-methyltransferase P21964
C0033937 Psychoses, Drug COMT 1312 catechol-O-methyltransferase P21964
C4552100 Lynch Syndrome COMT 1312 catechol-O-methyltransferase P21964
C0086543 Cataract COMT 1312 catechol-O-methyltransferase P21964
C0017601 Glaucoma COMT 1312 catechol-O-methyltransferase P21964
C0036439 Scoliosis, unspecified COMT 1312 catechol-O-methyltransferase P21964
C0039496 Temporomandibular Joint Dysfunction Syndrome COMT 1312 catechol-O-methyltransferase P21964
C0021122 Disruptive, Impulse Control, and Conduct Disorders COMT 1312 catechol-O-methyltransferase P21964
C0014170 Endometrial Neoplasms COMT 1312 catechol-O-methyltransferase P21964
C0752347 Lewy Body Disease COMT 1312 catechol-O-methyltransferase P21964
C0010417 Cryptorchidism COMT 1312 catechol-O-methyltransferase P21964
C0036939 Shared Paranoid Disorder COMT 1312 catechol-O-methyltransferase P21964

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Last updated: August 19, 2024