Disease #00050

Official abbreviation	PEOA6
Name	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 6, PEOA6
OMIM ID	615156
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	DNA2
Associated tissues	-
Disease features	-
Remarks	-