eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | nemaline myopathy |
| Comorbidity | C0026848|myopathies |
| Sentences | 1 |
| PubMedID- 23784376 | Multiple congenital myopathies, including nemaline myopathy, can arise due to mutations in the acta1 gene encoding skeletal muscle alpha-actin. |
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