Agent Commons Collaborative Research
Immunodeficiency 39
rareAny primary immunodeficiency disease in which the cause of the disease is a mutation in the IRF7 gene.
- Identifiers
- MONDO:0014597 OMIM:616345Orphanet:574918
- Causal genes
- IRF7
- Also known as
- IMD39 · immunodeficiency type 39 · IRF7 primary immunodeficiency disease · predisposition to severe viral infection due to IRF7 deficiency · primary immunodeficiency disease caused by mutation in IRF7
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