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 5726 - 5750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
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
C0023652 Lichen Sclerosus et Atrophicus CAT 847 catalase P04040
C0038013 Ankylosing spondylitis CAT 847 catalase P04040
C0079744 Diffuse Large B-Cell Lymphoma CAT 847 catalase P04040
C0206661 Gonadoblastoma CAT 847 catalase P04040
C0221757 alpha 1-Antitrypsin Deficiency CAT 847 catalase P04040
C0236663 Alcohol withdrawal syndrome CAT 847 catalase P04040
C0206115 WAGR Syndrome CAT 847 catalase P04040
C0339573 Glaucoma, Primary Open Angle CAT 847 catalase P04040
C1368683 Epithelioma CAT 847 catalase P04040
C0595989 Carcinoma of larynx CAT 847 catalase P04040
C0004153 Atherosclerosis CAT 847 catalase P04040
C0007758 Cerebellar Ataxia CAT 847 catalase P04040
C0023891 Liver Cirrhosis, Alcoholic CAT 847 catalase P04040
C0026691 Mucocutaneous Lymph Node Syndrome CAT 847 catalase P04040
C0034960 Refsum Disease CAT 847 catalase P04040
C0019163 Hepatitis B CAT 847 catalase P04040
C0432283 Osteoglophonic dwarfism CAT 847 catalase P04040

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Last updated: August 19, 2024