| Term Name: | nuclear type mitochondrial complex I deficiency 8 |
|---|---|
| Synonyms: | MC1DN8 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS3 gene on chromosome 11p11.2. |
| Ontology: | Human Disease [DOID:0112081] ( DOID:0112081 ) |