Term Name: nuclear type mitochondrial complex I deficiency 4
Synonyms: MC1DN4
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFV1 gene on chromosome 11q13.2.
Ontology: Human Disease [DOID:0112082]   ( DOID:0112082 )

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