1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0070505 | mitochondrial complex IV deficiency nuclear type 20 | A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX5A gene on chromosome 15q24.2. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
