| Term Name: | nuclear type mitochondrial complex I deficiency 34 |
|---|---|
| Synonyms: | MC1DN34 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF8 gene on chromosome 17q25.3. |
| Ontology: | Human Disease [DOID:0112091] ( DOID:0112091 ) |