Disease #00659 (PEOA5 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 5 (PEOA-5)), OMIM:613077)

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Official abbreviation	PEOA5
Name	ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 5 (PEOA-5)
OMIM ID	613077
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RRM2B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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