Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome | 79091 | MYH2 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |