Disease #00579

Official abbreviation	618120
Name	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5
OMIM ID	618120
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	ATP5F1D
Associated tissues	-
Disease features	-
Remarks	-