| DISEASE NAME | Congenital fiber-type disproportion myopathy |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | 255310; 300580; 617760; 601493; 601494; 604169; 609470; 611878; 613424; 613426; 615092; 615373; 615396 |
| 1 combination linked to 2020 | OLI123 |
| 1 gene combination linked to 2020 | ITGA7; MYH7B |
| ORPHANET ID | 2020 |