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 54251 - 54275 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0282513 Primary Progressive Aphasia (disorder) CAT 847 catalase P04040
C0030354 Papilloma CAT 847 catalase P04040
C0162532 Variegate Porphyria CAT 847 catalase P04040
C0031039 Pericardial effusion CAT 847 catalase P04040
C0030246 Pustulosis of Palms and Soles CAT 847 catalase P04040
C1868598 PARIETAL FORAMINA CAT 847 catalase P04040
C0259783 mixed gliomas CAT 847 catalase P04040
C1168401 Squamous cell carcinoma of the head and neck CAT 847 catalase P04040
C0678222 Breast Carcinoma CANX 821 calnexin P27824
C0027651 Neoplasms CANX 821 calnexin P27824
C1704380 Distal Renal Tubular Acidosis CANX 821 calnexin P27824
C0026470 Monoclonal Gammopathy of Undetermined Significance CANX 821 calnexin P27824
C0524620 Metabolic Syndrome X CANX 821 calnexin P27824
C0004153 Atherosclerosis CANX 821 calnexin P27824
C0151744 Myocardial Ischemia CANX 821 calnexin P27824
C1306459 Primary malignant neoplasm CANX 821 calnexin P27824
C0041341 Tuberous Sclerosis CANX 821 calnexin P27824
C0025007 Measles CANX 821 calnexin P27824
C0006826 Malignant Neoplasms CANX 821 calnexin P27824
C0376358 Malignant neoplasm of prostate CANX 821 calnexin P27824
C0022595 Keratosis Follicularis CANX 821 calnexin P27824
C0014553 Absence Epilepsy CANX 821 calnexin P27824
C0007959 Charcot-Marie-Tooth Disease CANX 821 calnexin P27824
C0006142 Malignant neoplasm of breast CANX 821 calnexin P27824
C0442874 Neuropathy CANX 821 calnexin P27824

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Last updated: August 19, 2024