| Term Name: | nuclear type mitochondrial complex I deficiency 19 |
|---|---|
| Synonyms: | MC1DN19 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the FOXRED1 gene on chromosome 11q24.2. |
| Ontology: | Human Disease [DOID:0112085] ( DOID:0112085 ) |