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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
myotonic disease
Summary
- Definition
- A muscular dystrophy that is characterized by progressive muscle wasting and weakness.
- Super Class
- muscular dystrophy
External Links
- Disease Ontology
- DOID:450
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 250 | ALPP | alkaline phosphatase, placental | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 3339 | HSPG2 | heparan sulfate proteoglycan 2 | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 4360 | MRC1 | mannose receptor C-type 1 | |
| 4534 | MTM1 | myotubularin 1 | |
| 5226 | PGD | phosphogluconate dehydrogenase | |
| 5563 | PRKAA2 | protein kinase AMP-activated catalytic subunit alpha 2 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 7368 | UGT8 | UDP glycosyltransferase 8 |
Related Glycoprotein
