Term Name: nuclear type mitochondrial complex I deficiency 23
Synonyms: MC1DN23
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA12 gene on chromosome 12q22.
Ontology: Human Disease [DOID:0112087]   ( DOID:0112087 )

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