Disease #01861 (CVID2 (immunodeficiency, variable, common, type 2 (CVID-2)), OMIM:240500)

Global Variome shared LOVD

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Official abbreviation	CVID2
Name	immunodeficiency, variable, common, type 2 (CVID-2)
OMIM ID	240500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 5 genes	CD19, CR2, ICOS, TNFRSF13B, TNFRSF13C
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)

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