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 53451 - 53475 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0020503 Hyperparathyroidism, Secondary UMOD 7369 uromodulin P07911
C0282488 Interstitial Cystitis UMOD 7369 uromodulin P07911
C0023452 Childhood Acute Lymphoblastic Leukemia UMOD 7369 uromodulin P07911
C0948008 Ischemic stroke UMOD 7369 uromodulin P07911
C0005684 Malignant neoplasm of urinary bladder UMOD 7369 uromodulin P07911
C1332977 Childhood Leukemia UMOD 7369 uromodulin P07911
C0085548 Autosomal Recessive Polycystic Kidney Disease UMOD 7369 uromodulin P07911
C0024138 Lupus Erythematosus, Discoid UMOD 7369 uromodulin P07911
C0376358 Malignant neoplasm of prostate UMPS 7372 uridine monophosphate synthetase P11172
C0085578 Thalassemia Minor UMPS 7372 uridine monophosphate synthetase P11172
C0027651 Neoplasms UMPS 7372 uridine monophosphate synthetase P11172
C0027947 Neutropenia UMPS 7372 uridine monophosphate synthetase P11172
C0007131 Non-Small Cell Lung Carcinoma UMPS 7372 uridine monophosphate synthetase P11172
C0011991 Diarrhea UMPS 7372 uridine monophosphate synthetase P11172
C1306459 Primary malignant neoplasm UMPS 7372 uridine monophosphate synthetase P11172
C0152018 Esophageal carcinoma UMPS 7372 uridine monophosphate synthetase P11172
C0038356 Stomach Neoplasms UMPS 7372 uridine monophosphate synthetase P11172
C0268130 Hereditary orotic aciduria, type 1 UMPS 7372 uridine monophosphate synthetase P11172
C0009402 Colorectal Carcinoma UMPS 7372 uridine monophosphate synthetase P11172
C0279626 Squamous cell carcinoma of esophagus UMPS 7372 uridine monophosphate synthetase P11172
C1708349 Hereditary Diffuse Gastric Cancer UMPS 7372 uridine monophosphate synthetase P11172
C0007137 Squamous cell carcinoma UMPS 7372 uridine monophosphate synthetase P11172
C0949116 Congenital hypoplastic anemia UMPS 7372 uridine monophosphate synthetase P11172
C1956346 Coronary Artery Disease UMPS 7372 uridine monophosphate synthetase P11172
C0009404 Colorectal Neoplasms UMPS 7372 uridine monophosphate synthetase P11172

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Last updated: August 19, 2024