PedAM
Pediatric Disease Annotations & Medicines
| Disease | muscular atrophy |
| Phenotype | C0751778|progressive myoclonic epilepsy |
| Sentences | 4 |
| PubMedID- 24164096 | Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy. |
| PubMedID- 25847462 | Spinal muscular atrophy associated with progressive myoclonic epilepsy: a rare condition caused by mutations in asah1. |
| PubMedID- 22703880 | Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in asah1. |
| PubMedID- 26526000 | Spinal muscular atrophy with progressive myoclonic epilepsy (sma-pme) is an extremely rare disorder related to the lysosomal storage disease, farber lipogranulomatosis. |
Page: 1