Disease #00025

Official abbreviation	614053
Name	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, 614053 (3)
OMIM ID	614053
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	ATP5E, ATP5F1E
Associated tissues	-
Disease features	-
Remarks	-