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 51926 - 51950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0155877 Allergic asthma AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0034735 Raynaud Phenomenon AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0004153 Atherosclerosis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0020071 Hereditary Sensory Autonomic Neuropathy, Type 1 AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0035078 Kidney Failure AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0162311 Androgenetic Alopecia AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0021775 Intermittent Claudication AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0020500 Hyperoxaluria AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0011603 Dermatitis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0042109 Urticaria AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0004245 Atrioventricular Block AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0004096 Asthma AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0221232 Welts AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0027709 Nephrocalcinosis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0392525 Nephrolithiasis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0268646 Isolated cystinuria AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C4721453 Peripheral Nervous System Diseases AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0013595 Eczema AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0017636 Glioblastoma AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0018889 Helminthiasis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0264995 Occlusion of artery (disorder) AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0014122 Subacute Bacterial Endocarditis AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C1561643 Chronic Kidney Diseases AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0279980 Extra-osseous Ewing's sarcoma AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0025517 Metabolic Diseases AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549

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Last updated: August 19, 2024