Disease #02611 (HIGM3 (immunodeficiency, with hyper IgM, type 3 (HIGM-3)), OMIM:606843)

Official abbreviation HIGM3
Name immunodeficiency, with hyper IgM, type 3 (HIGM-3)
OMIM ID 606843
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene CD40
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     
00046596 - - - M - Tunisia - - - - - HIGM3 - CD40 CD40 1 1 Hanen Ouadani
Legend   How to query  


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