1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111524 | autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the TOP3A gene on chromosome 17p11.2. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080000 | muscular disease | A musculoskeletal system disease that affects the muscles. |
