| Term Name: | nuclear type mitochondrial complex I deficiency 2 |
|---|---|
| Synonyms: | MC1DN2 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS8 gene on chromosome 11q13.2. |
| Ontology: | Human Disease [DOID:0112083] ( DOID:0112083 ) |