| Term Name: | nuclear type mitochondrial complex I deficiency 15 |
|---|---|
| Synonyms: | MC1DN15 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF4 gene on chromosome 6q16.1. |
| Ontology: | Human Disease [DOID:0112077] ( DOID:0112077 ) |