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 45076 - 45100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0018780 Hearing Loss, High-Frequency CAT 847 catalase P04040
C0003873 Rheumatoid Arthritis CAT 847 catalase P04040
C0003949 Asbestosis CAT 847 catalase P04040
C0282526 Hyperpipecolic Acidemia CAT 847 catalase P04040
C0036202 Sarcoidosis CAT 847 catalase P04040
C1561643 Chronic Kidney Diseases CAT 847 catalase P04040
C0022665 Kidney Neoplasm CAT 847 catalase P04040
C3875321 Inflammatory dermatosis CAT 847 catalase P04040
C0004943 Behcet Syndrome CAT 847 catalase P04040
C0001973 Alcoholic Intoxication, Chronic CAT 847 catalase P04040
C0027819 Neuroblastoma CAT 847 catalase P04040
C1269683 Major Depressive Disorder CAT 847 catalase P04040
C2711227 Steatohepatitis CAT 847 catalase P04040
C0029882 Otitis Media CAT 847 catalase P04040
C0038354 Stomach Diseases CAT 847 catalase P04040
C0010054 Coronary Arteriosclerosis CAT 847 catalase P04040
C0282527 Infantile Refsum Disease (disorder) CAT 847 catalase P04040
C0086795 Pfaundler-Hurler Syndrome CAT 847 catalase P04040
C0027022 Myeloproliferative disease CAT 847 catalase P04040
C0022610 Kernicterus CAT 847 catalase P04040
C0282525 Adrenoleukodystrophy, Neonatal CAT 847 catalase P04040
C0043208 Wolman Disease CAT 847 catalase P04040
C3714636 Pneumonitis CAT 847 catalase P04040
C0043119 Werner Syndrome CAT 847 catalase P04040
C0014070 Encephalomyelitis CAT 847 catalase P04040

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Last updated: August 19, 2024