Term Name: mitochondrial complex V (ATP synthase) deficiency nuclear type 1
Synonyms: MC5DN1
Definition: A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATPAF2 gene on chromosome 17p11.
Ontology: Human Disease [DOID:0050768]   ( DOID:0050768 )

Relationships
is a type of: mitochondrial complex V (ATP synthase) deficiency