eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | gne myopathy |
| Comorbidity | C0002736|amyotrophic lateral sclerosis |
| Sentences | 1 |
| PubMedID- 25545721 | Mutations in the vcp gene have also been associated with amyotrophic lateral sclerosis in 10-15% of individuals with hereditary inclusion body myopathy and 2-3% of isolated familial amyotrophic lateral sclerosis. |
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