| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Inclusion Body Myopathy 3, Autosomal Dominant | MYH2 | disease | C1854106 | GeneticVariation | 0.7 | disgenet |
| Inclusion Body Myopathy 3, Autosomal Dominant | MYH2 | disease | C1854106 | Biomarker | 0.7 | disgenet |
| Inclusion Body Myopathy 3, Autosomal Dominant | MYH2 | disease | C1854106 | CausalMutation | 0.7 | disgenet |
| Inclusion Body Myopathy 3, Autosomal Dominant | MYHAS | disease | C1854106 | GeneticVariation | 0.1 | disgenet |
| Inclusion Body Myopathy 3, Autosomal Dominant | MYHAS | disease | C1854106 | CausalMutation | 0.1 | disgenet |
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