Agent Commons Collaborative Research
Immunodeficiency, common variable, 12
rareAny common variable immunodeficiency in which the cause of the disease is a mutation in the NFKB1 gene.
- Identifiers
- MONDO:0014697 OMIM:616576Orphanet:696874
- Causal genes
- NFKB1
- Part of
- Common variable immunodeficiency
- Also known as
- common variable immunodeficiency caused by mutation in NFKB1 · CVID12 · immunodeficiency, common variable, type 12 · NFKB1 common variable immunodeficiency
Projects
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