Disease #00024

Official abbreviation	614052
Name	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3)
OMIM ID	614052
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TMEM70
Associated tissues	-
Disease features	-
Remarks	-