| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Myopathy, Actin, Congenital, with Excess of Thin Myofilaments | ACTA1 | disease | C1834339 | Biomarker | 0.6 | disgenet |
| Myopathy, Actin, Congenital, with Excess of Thin Myofilaments | ACTA1 | disease | C1834339 | CausalMutation | 0.6 | disgenet |
| Myopathy, Actin, Congenital, with Excess of Thin Myofilaments | IRF6 | disease | C1834339 | Biomarker | 0.2 | disgenet |
| Myopathy, Actin, Congenital, with Excess of Thin Myofilaments | GRHL3 | disease | C1834339 | Biomarker | 0.2 | disgenet |
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