1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080117 | mitochondrial complex III deficiency nuclear type 8 | A mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has_material_basis_in homozygous mutation in the LYRM7 gene on chromosome 5q23. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111139 | mitochondrial complex III deficiency | A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III. |
