PedAM
Pediatric Disease Annotations & Medicines
| Disease | myopathy |
| Phenotype | C0026848|myopathy |
| Sentences | 1 |
| PubMedID- 23671309 | Mutations in nebulin are responsible for nemaline myopathy, a group of congenital muscle disorders characterized by generalized muscle weakness and rod-like nemaline bodies in myofibers (wallgren-pettersson et al., 2011). |
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