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 45126 - 45150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0268381 Primary amyloidosis CAT 847 catalase P04040
C3250443 MYOTONIC DYSTROPHY 1 CAT 847 catalase P04040
C1571983 Involutional paraphrenia CAT 847 catalase P04040
C0017605 Angle Closure Glaucoma CAT 847 catalase P04040
C0007222 Cardiovascular Diseases CAT 847 catalase P04040
C0948008 Ischemic stroke CAT 847 catalase P04040
C0206698 Cholangiocarcinoma CAT 847 catalase P04040
C0019159 Hepatitis A CAT 847 catalase P04040
C0154723 Migraine with Aura CAT 847 catalase P04040
C3469521 FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) CAT 847 catalase P04040
C0035078 Kidney Failure CAT 847 catalase P04040
C0023467 Leukemia, Myelocytic, Acute CAT 847 catalase P04040
C0271454 Chronic purulent otitis media CAT 847 catalase P04040
C0009324 Ulcerative Colitis CAT 847 catalase P04040
C0700095 Central neuroblastoma CAT 847 catalase P04040
C0003431 Antisocial Personality Disorder CAT 847 catalase P04040
C0751753 Carbamoyl-Phosphate Synthase I Deficiency Disease CAT 847 catalase P04040
C0400966 Non-alcoholic Fatty Liver Disease CAT 847 catalase P04040
C0029408 Degenerative polyarthritis CAT 847 catalase P04040
C0032290 Aspiration Pneumonia CAT 847 catalase P04040
C0339277 Corneal Dystrophy, Juvenile Epithelial of Meesmann CAT 847 catalase P04040
C0033141 Cardiomyopathies, Primary CAT 847 catalase P04040
C1862941 Amyotrophic Lateral Sclerosis, Sporadic CAT 847 catalase P04040
C0555198 Malignant Glioma CAT 847 catalase P04040
C0023452 Childhood Acute Lymphoblastic Leukemia CAT 847 catalase P04040

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Last updated: August 19, 2024