Term Name: nuclear type mitochondrial complex I deficiency 14
Synonyms: MC1DN14
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA11 gene on chromosome 19p13.3.
Ontology: Human Disease [DOID:0112094]   ( DOID:0112094 )

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