1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0112080 | nuclear type mitochondrial complex I deficiency 32 | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB8 gene on chromosome 10q24.31. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
