Disease #06359 (PEOB5 (?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5), OMIM:618098)

Official abbreviation	PEOB5
Name	?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5
OMIM ID	618098
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TOP3A
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