Disease #06460 (PEOB4 (Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 4), OMIM:617070)

Official abbreviation	PEOB4
Name	Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 4
OMIM ID	617070
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DGUOK
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