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 10601 - 10625 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C3489413 Lipomatosis, Multiple PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0243026 Sepsis PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0008370 Cholestasis PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0025517 Metabolic Diseases PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0206692 Carcinoma, Lobular PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0006142 Malignant neoplasm of breast PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0686353 Muscular Dystrophies, Limb-Girdle PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0242363 Islet Cell Tumor PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0017926 Glycogen Storage Disease Type VII PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0241005 Creatine phosphokinase serum increased PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0151744 Myocardial Ischemia PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0032914 Pre-Eclampsia PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0027080 Myoglobinuria PYGM 5837 glycogen phosphorylase, muscle associated P11217
C0017925 Glycogen Storage Disease Type VI PYGL 5836 glycogen phosphorylase L P06737
C2239176 Liver carcinoma PYGL 5836 glycogen phosphorylase L P06737
C0017495 Gerstmann-Straussler-Scheinker Disease PYGL 5836 glycogen phosphorylase L P06737
C0017920 Glycogen Storage Disease Type I PYGL 5836 glycogen phosphorylase L P06737
C0020615 Hypoglycemia PYGL 5836 glycogen phosphorylase L P06737
C0017924 Glycogen Storage Disease Type V PYGL 5836 glycogen phosphorylase L P06737
C0013336 Dwarfism PYGL 5836 glycogen phosphorylase L P06737
C0029438 Massive Osteolyses PYGL 5836 glycogen phosphorylase L P06737
C0017922 Glycogen Storage Disease Type III PYGL 5836 glycogen phosphorylase L P06737
C0155626 Acute myocardial infarction PYGB 5834 glycogen phosphorylase B P11216
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PYGB 5834 glycogen phosphorylase B P11216
C0151744 Myocardial Ischemia PYGB 5834 glycogen phosphorylase B P11216

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Last updated: August 19, 2024