Term Name: nuclear type mitochondrial complex I deficiency 34
Synonyms: MC1DN34
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF8 gene on chromosome 17q25.3.
Ontology: Human Disease [DOID:0112091]   ( DOID:0112091 )

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