Disease #00049

Official abbreviation	PEOA5
Name	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5, PEOA5
OMIM ID	613077
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	RRM2B
Associated tissues	-
Disease features	-
Remarks	-