PedAM
Pediatric Disease Annotations & Medicines
| Disease | lateral sclerosis |
| Phenotype | C0026848|myopathy |
| Sentences | 1 |
| PubMedID- 26208961 | Similar to mutations in vcp, dominantly inherited mutations in sqstm1 are now associated with rimmed vacuolar myopathy, paget disease of bone, amyotrophic lateral sclerosis, and frontotemporal dementia. |
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