| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Inclusion body myopathy, autosomal dominant | MYH2 | disease | C2931820 | GeneticVariation | 0.03 | disgenet |
| Inclusion body myopathy, autosomal dominant | VCP | disease | C2931820 | GeneticVariation | 0.03 | disgenet |
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