Term Name: nuclear type mitochondrial complex I deficiency 18
Synonyms: MC1DN18
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF3 gene on chromosome 2p21.31.
Ontology: Human Disease [DOID:0112070]   ( DOID:0112070 )

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