Disease #02536 (HIGM2 (immunodeficiency, with hyper IgM, type 2 (HIGM-2)), OMIM:605258)

Official abbreviation HIGM2
Name immunodeficiency, with hyper IgM, type 2 (HIGM-2)
OMIM ID 605258
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 10
Phenotype entries for this disease 7
Associated with 1 gene AICDA
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

10 entries on 1 page. Showing entries 1 - 10.
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00046593 - - - M no Tunisia - - - - - HIGM2 - AICDA AICDA 1 1 Hanen Ouadani
00046594 - - - - no Tunisia - - - - - HIGM2 - AICDA AICDA 1 5 Hanen Ouadani
00046595 - - - - - Tunisia - - - - - HIGM2 - AICDA AICDA 1 5 Hanen Ouadani
00058568 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - F no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058569 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - M no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058570 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - F no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058572 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - F no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058573 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - M no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058574 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - F no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
00058575 - Trotta 2016, submitted to EJHG (845-15-EJHGR) - M no Finland - - - - - HIGM2 - AICDA AICDA 1 1 Luca Trotta
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