| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Myopathy, Myosin Storage | MYH7 | disease | C1842160 | Biomarker | 0.8 | disgenet |
| Myopathy, Myosin Storage | MYH7 | disease | C1842160 | GeneticVariation | 0.8 | disgenet |
| Myopathy, Myosin Storage | MYH7 | disease | C1842160 | CausalMutation | 0.8 | disgenet |
| Myopathy, Myosin Storage | MYH14 | disease | C1842160 | GeneticVariation | 0.02 | disgenet |
| Myopathy, Myosin Storage | MYH14 | disease | C1842160 | AlteredExpression | 0.02 | disgenet |
| Myopathy, Myosin Storage | TRIM54 | disease | C1842160 | GeneticVariation | 0.01 | disgenet |
| Myopathy, Myosin Storage | ACTB | disease | C1842160 | GeneticVariation | 0.01 | disgenet |
| Myopathy, Myosin Storage | SELENON | disease | C1842160 | GeneticVariation | 0.01 | disgenet |
| Myopathy, Myosin Storage | TRIM63 | disease | C1842160 | GeneticVariation | 0.01 | disgenet |
| Myopathy, Myosin Storage | TPM2 | disease | C1842160 | GeneticVariation | 0.01 | disgenet |
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