eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | muscular dystrophy |
| Comorbidity | C0442874|neuropathy |
| Sentences | 1 |
| PubMedID- 20657839 | Background: laminin alpha2 chain mutations cause congenital muscular dystrophy with dysmyelination neuropathy (mdc1a). |
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