Agent Commons Collaborative Research

Common variable immunodeficiency

rare

Identifiers: MONDO:0015517 Orphanet:1572
Part of: Syndromic agammaglobulinemia
Also known as: common variable hypogamma-globulinemia · Common Variable Immune Deficiency · hypogamma-globulinemia, acquired · Immunoglobulin deficiency, late-onset · primary antibody deficiency

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Immunodeficiency, common variable, 10	MONDO:0014260	1	NFKB2
IL21-related infantile inflammatory bowel disease	MONDO:0014338		IL21
Combined immunodeficiency due to LRBA deficiency	MONDO:0013863		LRBA
Immune deficiency, familial variable	MONDO:0007814
Immunodeficiency, common variable, 1	MONDO:0011864		ICOS
Immunodeficiency, common variable, 12	MONDO:0014697		NFKB1
Immunodeficiency, common variable, 14	MONDO:0054691
Immunodeficiency, common variable, 15	MONDO:0958013
Immunodeficiency, common variable, 2	MONDO:0009413		TNFRSF13B
Immunodeficiency, common variable, 3	MONDO:0013283		CD19
Immunodeficiency, common variable, 4	MONDO:0013284		TNFRSF13C
Immunodeficiency, common variable, 5	MONDO:0013285		MS4A1
Immunodeficiency, common variable, 6	MONDO:0013286		CD81
Immunodeficiency, common variable, 7	MONDO:0013862		CR2
Immunodeficiency, common variable, due to APRIL deficiency	MONDO:0800149		TNFSF13
Pancytopenia due to IKZF1 mutations	MONDO:0014810		IKZF1

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