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Immunodeficiency 28

MONDO:0013953

Any primary immunodeficiency disease in which the cause of the disease is a mutation in the IFNGR2 gene.

Also known as: IFNGR2 primary immunodeficiency disease, immunodeficiency 28, immunodeficiency type 28, primary immunodeficiency disease caused by mutation in IFNGR2, IMD28, Ifngr2 deficiency, immunodeficiency 28, Mycobacteriosis

41 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 28 itself.

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Part of

↑ Hereditary disease (18187) ↑ Inborn error of immunity (343)

Including sub-types (41) Tagged with Immunodeficiency 28 (0)

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