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 54076 - 54100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0035344 Retinopathy of Prematurity CAT 847 catalase P04040
C1861172 Venous Thromboembolism CAT 847 catalase P04040
C0023493 Adult T-Cell Lymphoma/Leukemia CAT 847 catalase P04040
C3539168 PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A CAT 847 catalase P04040
C0281658 Intraocular Lymphoma CAT 847 catalase P04040
C0524702 Pulmonary Thromboembolisms CAT 847 catalase P04040
C0267917 Acute cholangitis CAT 847 catalase P04040
C0002895 Anemia, Sickle Cell CAT 847 catalase P04040
C0917805 Transient Cerebral Ischemia CAT 847 catalase P04040
C0025517 Metabolic Diseases CAT 847 catalase P04040
C0018213 Graves Disease CAT 847 catalase P04040
C0016667 Fragile X Syndrome CAT 847 catalase P04040
C0007097 Carcinoma CAT 847 catalase P04040
C1260386 Glucocorticoid-remediable aldosteronism CAT 847 catalase P04040
C0234535 Clonic Seizures CAT 847 catalase P04040
C0018784 Sensorineural Hearing Loss (disorder) CAT 847 catalase P04040
C0684249 Carcinoma of lung CAT 847 catalase P04040
C0205734 Diabetes, Autoimmune CAT 847 catalase P04040
C0023786 Mucopolysaccharidosis I CAT 847 catalase P04040
C0233794 Memory impairment CAT 847 catalase P04040
C0023524 Leukoencephalopathy, Progressive Multifocal CAT 847 catalase P04040
C0079541 Holoprosencephaly CAT 847 catalase P04040
C0005586 Bipolar Disorder CAT 847 catalase P04040
C0015695 Fatty Liver CAT 847 catalase P04040
C0276496 Familial Alzheimer Disease (FAD) CAT 847 catalase P04040

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Last updated: August 19, 2024