C176805Level 7
Interferon Gamma Receptor 2 Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** A genetic condition caused by mutation(s) in the IFNGR2 gene, encoding interferon gamma receptor 2, resulting in impairment of interferon-gamma mediated immunity. Clinically, it is characterized by predisposition to illness caused by moderately virulent mycobacterial species.
**Synonyms:** - IFNGR 2 Deficiency - IFNGR2 Deficiency
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