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 45901 - 45925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C1832370 MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED MTM1 4534 myotubularin 1 Q13496
C0006142 Malignant neoplasm of breast MTM1 4534 myotubularin 1 Q13496
C0162292 External Ophthalmoplegia MTM1 4534 myotubularin 1 Q13496
C0035220 Respiratory Distress Syndrome, Newborn MTM1 4534 myotubularin 1 Q13496
C0427055 Facial Paresis MTM1 4534 myotubularin 1 Q13496
C0036572 Seizures MTM1 4534 myotubularin 1 Q13496
C1456418 Absence of muscle MTM1 4534 myotubularin 1 Q13496
C0011847 Diabetes MTM1 4534 myotubularin 1 Q13496
C0524851 Neurodegenerative Disorders MTM1 4534 myotubularin 1 Q13496
C0027126 Myotonic Dystrophy MTM1 4534 myotubularin 1 Q13496
C0034494 Rabies (disorder) MTM1 4534 myotubularin 1 Q13496
C0011849 Diabetes Mellitus MTM1 4534 myotubularin 1 Q13496
C1306459 Primary malignant neoplasm MTM1 4534 myotubularin 1 Q13496
C0020224 Polyhydramnios MTM1 4534 myotubularin 1 Q13496
C0022661 Kidney Failure, Chronic MTM1 4534 myotubularin 1 Q13496
C0751401 Ophthalmoparesis MTM1 4534 myotubularin 1 Q13496
C0034194 Pyloric Stenosis MTM1 4534 myotubularin 1 Q13496
C0011334 Dental caries MTM1 4534 myotubularin 1 Q13496
C0011991 Diarrhea MTM1 4534 myotubularin 1 Q13496
C0442874 Neuropathy MTM1 4534 myotubularin 1 Q13496
C0014121 Bacterial Endocarditis MTM1 4534 myotubularin 1 Q13496
C0027868 Neuromuscular Diseases MTM1 4534 myotubularin 1 Q13496
C1541923 Infective endocarditis MTM1 4534 myotubularin 1 Q13496
C0270960 Congenital myopathy (disorder) MTM1 4534 myotubularin 1 Q13496
C0008372 Intrahepatic Cholestasis MTM1 4534 myotubularin 1 Q13496

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Last updated: August 19, 2024