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Disease Ontology Browser
immunodeficiency 33 (DOID:0112003)
Alliance: disease page
Synonyms: IMD33; X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency; X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency; X-linked MSMD due to IKBKG deficiency; X-linked MSMD due to NEMO deficiency
Alt IDs: OMIM:300636, MESH:C567070
Definition: A combined immunodeficiency characterized by early-onset severe infection and variable immunological abnormalities that has_material_basis_in hemizygous mutation in the IKBKG gene on chromosome Xq28.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory