Disease #00023

Official abbreviation	604273
Name	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, 604273 (3)
OMIM ID	604273
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	ATPAF2
Associated tissues	-
Disease features	-
Remarks	-