Disease #00041 (PEOA3 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 3 (PEOA-3)), OMIM:609286)

Official abbreviation PEOA3
Name ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 3 (PEOA-3)
OMIM ID 609286
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene C10orf2
Associated tissues -
Disease features -
Remarks -
Date created 2012-08-30 16:46:02 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00276000 - - - - ? Spain - - - - - PEOA3 - C10orf2 C10orf2 1 1 Pablo Serrano-Lorenzo
00276002 - - - - ? Spain - - - - - PEOA3 - C10orf2 C10orf2 1 1 Pablo Serrano-Lorenzo
00380802 ? PubMed: Nair 2018 - ? - Lebanon - - - - - PEOA3 ID; muscle weakness; seizures; decreased mitochondrial respiratory chain complex activity (Neurological) - C10orf2 1 1 LOVD
Legend   How to query  


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