Disease #04646 (PEOB2 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal recessive, type 2 (PEOB-2)), OMIM:616479)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	PEOB2
Name	ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal recessive, type 2 (PEOB-2)
OMIM ID	616479
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RNASEH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.