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 57076 - 57100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0011875 Diabetic Angiopathies CAT 847 catalase P04040
C0008350 Cholelithiasis CAT 847 catalase P04040
C0008370 Cholestasis CAT 847 catalase P04040
C0021831 Intestinal Diseases CAT 847 catalase P04040
C0220668 Congenital contractural arachnodactyly CAT 847 catalase P04040
C0026847 Spinal Muscular Atrophy CAT 847 catalase P04040
C0015696 Fatty Liver, Alcoholic CAT 847 catalase P04040
C0752121 Spinocerebellar Ataxia Type 2 CAT 847 catalase P04040
C0220748 Cartilage-hair hypoplasia CAT 847 catalase P04040
C0009402 Colorectal Carcinoma CAT 847 catalase P04040
C0034065 Pulmonary Embolism CAT 847 catalase P04040
C0079474 Hallopeau-Siemens Disease CAT 847 catalase P04040
C0025289 Meningitis CAT 847 catalase P04040
C0085084 Motor Neuron Disease CAT 847 catalase P04040
C0015934 Fetal Growth Retardation CAT 847 catalase P04040
C0023530 Leukopenia CAT 847 catalase P04040
C0025958 Microcephaly CAT 847 catalase P04040
C0007131 Non-Small Cell Lung Carcinoma CAT 847 catalase P04040
C0009375 Colonic Neoplasms CAT 847 catalase P04040
C0520947 Clumsiness - motor delay CAT 847 catalase P04040
C0205770 Choroid Plexus Papilloma CAT 847 catalase P04040
C0406810 Carney Complex CAT 847 catalase P04040
C0917796 Optic Atrophy, Hereditary, Leber CAT 847 catalase P04040
C0019189 Hepatitis, Chronic CAT 847 catalase P04040
C0036646 Age-related cataract CAT 847 catalase P04040

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Last updated: August 19, 2024