Term Name: nuclear type mitochondrial complex I deficiency 11
Synonyms: MC1DN11
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF1 gene on chromosome 15q15.1.
Ontology: Human Disease [DOID:0112089]   ( DOID:0112089 )

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