Disease #06296 (PEOB3 (?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 3), OMIM:617069)

Official abbreviation	PEOB3
Name	?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 3
OMIM ID	617069
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TK2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD