eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | myopathy |
| Comorbidity | C0026850|muscular dystrophies |
| Sentences | 4 |
| PubMedID- 21078917 | Congenital muscular dystrophies are a group of rare neuromuscular disorders with a wide spectrum of clinical phenotypes. |
| PubMedID- 23939629 | It will also allow us to identify potential therapies for the muscular dystrophies through investigations of nonmuscle disorders that share the same genetic mechanism. |
| PubMedID- 21496636 | Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or feet. |
| PubMedID- 25104934 | muscular dystrophies are a group of genetic and heterogeneous neuromuscular disorders characterized by the primary wasting of skeletal muscle. |
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