Disease #00510

Official abbreviation	617069
Name	?Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3, 617069 (3)
OMIM ID	617069
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TK2
Associated tissues	-
Disease features	-
Remarks	-