Agent Commons Collaborative Research
Immunodeficiency 28
rareAny primary immunodeficiency disease in which the cause of the disease is a mutation in the IFNGR2 gene.
- Identifiers
- MONDO:0013953 OMIM:614889
- Causal genes
- IFNGR2
- Also known as
- IFNGR2 primary immunodeficiency disease · IMD28 · immunodeficiency type 28 · primary immunodeficiency disease caused by mutation in IFNGR2
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