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 5801 - 5825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0029531 Other cataract CAT 847 catalase P04040
C0085179 Eosinophilia-Myalgia Syndrome CAT 847 catalase P04040
C0022578 Keratoconus CAT 847 catalase P04040
C0027051 Myocardial Infarction CAT 847 catalase P04040
C0032002 Pituitary Diseases CAT 847 catalase P04040
C0085580 Essential Hypertension CAT 847 catalase P04040
C0031485 Phenylketonurias CAT 847 catalase P04040
C0699791 Stomach Carcinoma CAT 847 catalase P04040
C0085576 Iron-Refractory Iron Deficiency Anemia CAT 847 catalase P04040
C0019158 Hepatitis CAT 847 catalase P04040
C0038358 Gastric ulcer CAT 847 catalase P04040
C0010692 Cystitis CAT 847 catalase P04040
C3160718 PARKINSON DISEASE, LATE-ONSET CAT 847 catalase P04040
C0032131 Plasmacytoma CAT 847 catalase P04040
C0086132 Depressive Symptoms CAT 847 catalase P04040
C0031099 Periodontitis CAT 847 catalase P04040
C0031046 Pericarditis CAT 847 catalase P04040
C0035309 Retinal Diseases CAT 847 catalase P04040
C0004509 Azoospermia CAT 847 catalase P04040
C0021670 insulinoma CAT 847 catalase P04040
C0751434 Classical phenylketonuria CAT 847 catalase P04040
C0019202 Hepatolenticular Degeneration CAT 847 catalase P04040
C0017636 Glioblastoma CAT 847 catalase P04040
C0001815 Primary Myelofibrosis CAT 847 catalase P04040
C0033575 Prostatic Diseases CAT 847 catalase P04040

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Last updated: August 19, 2024