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 8751 - 8775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C2752147 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C CAT 847 catalase P04040
C0268263 Multiple Sulfatase Deficiency Disease CAT 847 catalase P04040
C0149519 Chronic Persistent Hepatitis CAT 847 catalase P04040
C1837218 Cleft palate, isolated CAT 847 catalase P04040
C0003504 Aortic Valve Insufficiency CAT 847 catalase P04040
C0001339 Acute pancreatitis CAT 847 catalase P04040
C0242380 Libman-Sacks Disease CAT 847 catalase P04040
C0235032 Neurotoxicity Syndromes CAT 847 catalase P04040
C1275685 Avellino corneal dystrophy CAT 847 catalase P04040
C0036221 Mast-Cell Sarcoma CAT 847 catalase P04040
C0004238 Atrial Fibrillation CAT 847 catalase P04040
C0001261 Actinomycosis CAT 847 catalase P04040
C0026269 Mitral Valve Stenosis CAT 847 catalase P04040
C0740394 Hyperuricemia CAT 847 catalase P04040
C1332979 Childhood Lymphoma CAT 847 catalase P04040
C0027859 Acoustic Neuroma CAT 847 catalase P04040
C1258104 Diffuse Scleroderma CAT 847 catalase P04040
C0162830 Dermatitis, Phototoxic CAT 847 catalase P04040
C0027583 Nematode infections CAT 847 catalase P04040
C0520463 Chronic active hepatitis CAT 847 catalase P04040
C0014733 Erysipelas CAT 847 catalase P04040
C0005695 Bladder Neoplasm CAT 847 catalase P04040
C0339543 Epiretinal Membrane CAT 847 catalase P04040
C0271686 Diabetic Autonomic Neuropathy CAT 847 catalase P04040
C0162316 Iron deficiency anemia CAT 847 catalase P04040

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Last updated: August 19, 2024