eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | myopathy |
| Comorbidity | C0026846|muscular atrophy |
| Sentences | 4 |
| PubMedID- 22776143 | An autosomal recessive neuromuscular disease, spinal muscular atrophy is the leading genetic cause of mortality in children. |
| PubMedID- 24125563 | Sporadic inclusion body myositis (sibm) is a slowly progressive, red-rimmed vacuolar myopathy leading to muscular atrophy and progressive weakness; it predominantly affects males older than fifty years, and is resistant to immunotherapy. |
| PubMedID- 24876969 | Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment tool. |
| PubMedID- 20800519 | Background: spinal muscular atrophy is one of the most common neuromuscular disorders in children. |
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