Disease #01027 (DCHE (deafness, congenital heart defects, posterior embryotoxon (DCHE)), OMIM:617992)

Official abbreviation DCHE
Name deafness, congenital heart defects, posterior embryotoxon (DCHE)
OMIM ID 617992
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene JAG1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-06-07 11:51:21 +02:00 (CEST)


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     
00239595 - PubMed: Le Caignec 2002 - - - - - - - - - DCHE see paper; … JAG1 JAG1 1 1 Johan den Dunnen
Legend   How to query  


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