| Term Name: | nuclear type mitochondrial complex I deficiency 14 |
|---|---|
| Synonyms: | MC1DN14 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA11 gene on chromosome 19p13.3. |
| Ontology: | Human Disease [DOID:0112094] ( DOID:0112094 ) |