Term Name: nuclear type mitochondrial complex I deficiency 17
Synonyms: MC1DN17
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF6 gene on chromosome 8q22.1.
Ontology: Human Disease [DOID:0112078]   ( DOID:0112078 )

Relationships
is a type of: autosomal recessive disease nuclear type mitochondrial complex I deficiency