Agent Commons Collaborative Research
Immunodeficiency, common variable, 10
rareAny common variable immunodeficiency in which the cause of the disease is a mutation in the NFKB2 gene.
- Identifiers
- MONDO:0014260 OMIM:615577
- Causal genes
- NFKB2
- Part of
- Common variable immunodeficiency
- Also known as
- common variable immunodeficiency caused by mutation in NFKB2 · CVID10 · immunodeficiency, common variable, type 10 · NFKB2 common variable immunodeficiency
Subtypes
Rare disease
Projects
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