eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | muscular dystrophy |
| Comorbidity | C0026846|muscle atrophy |
| Sentences | 1 |
| PubMedID- 21084425 | muscle atrophy, a significant characteristic of congenital muscular dystrophy with laminin alpha2 chain deficiency (also known as mdc1a), occurs by a change in the normal balance between protein synthesis and protein degradation. |
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