Disease #03048 (COXPD5 (combined oxidative phosphorylation deficiency, type 5 (COXPD-5)), OMIM:611719)

Official abbreviation COXPD5
Name combined oxidative phosphorylation deficiency, type 5 (COXPD-5)
OMIM ID 611719
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MRPS22
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
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     
00095093 - - - - no - - - - - - COXPD5 Agenesis of corpus callosum, Hypertrophic cardiomyopathy, Pulmonary hypoplasia, Low-set ears - MRPS22 2 1 Karen Stals
Legend   How to query  


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