| Term Name: | nuclear type mitochondrial complex I deficiency 27 |
|---|---|
| Synonyms: | MC1DN27 |
| Definition: | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MTFMT gene on chromosome 15q22.31. |
| Ontology: | Human Disease [DOID:0112090] ( DOID:0112090 ) |