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 |
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