Disease #02243 (HIGM1 (immunodeficiency, with hyper IgM, type 1 (HIGM-1)), OMIM:308230)

Official abbreviation HIGM1
Name immunodeficiency, with hyper IgM, type 1 (HIGM-1)
OMIM ID 308230
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CD40LG
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

3 entries on 1 page. Showing entries 1 - 3.
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00046850 - - - M - Tunisia - - - - - HIGM1 X-Linked hyper IgM CD40LG CD40LG 1 1 Hanen Ouadani
00046851 - - - M no Tunisia - - - - - HIGM1 X-Linked hyper IgM CD40LG CD40LG 1 1 Hanen Ouadani
00046852 - - - M no Tunisia - - - - - HIGM1 X-Linked hyper IgM CD40LG CD40LG 1 1 Hanen Ouadani
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