Immunodeficiency 33

MONDO:0010386

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

Also known as: IKBKG X-linked mendelian susceptibility to mycobacterial diseases, IKBKG invasive pneumococcal disease, recurrent isolated, IMD33, IPD2, X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in IKBKG, immunodeficiency 33, Mycobacteriosis, X-linked, immunodeficiency 33, X-linked recessive, immunodeficiency type 33

41 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 33 itself.

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Part of

↑ Inborn error of immunity (345) ↑ IKBKG-related immunodeficiency with or without ectodermal dysplasia (4)

Including sub-types (41) Tagged with Immunodeficiency 33 (0)

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