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 59526 - 59550 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0271093 Stargardt's disease AKR1A1 10327 aldo-keto reductase family 1 member A1 P14550
C0022650 Kidney Calculi AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C2239176 Liver carcinoma AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0020501 Primary Hyperoxaluria AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
C0010691 Cystinuria AGXT 189 alanine--glyoxylate and serine--pyruvate aminotransferase P21549
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

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Last updated: August 19, 2024