mitochondrial complex v (atp synthase) deficiency, nuclear type 1 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A mitochondrial metabolism disease that has material basis in mutation in the ATPAF2 gene on chromosome 17p11. (Human Disease Ontology, DOID_0050768)
External Link http://www.omim.org/entry/604273
Similar Terms
Downloads & Tools

Genes

1 genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ATPAF2 ATP synthase mitochondrial F1 complex assembly factor 2