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immunodeficiency 29 (DOID:0111950)
Alliance: disease page
Synonyms: IL12B deficiency; IMD29; immunodeficiency 29, mycobacteriosis; Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency; Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency; MSMD due to complete IL12B deficiency; MSMD due to complete interleukin 12B deficiency
Alt IDs: OMIM:614890, ORDO:319558
Definition: A primary immunodeficiency disease characterized by undetectable IL12B secretion by leukocytes and increased susceptibility to intracellular bacterial infections that has_material_basis_in homozygous or compound heterozygous mutation in IL12B on chromosome 5q33.3.


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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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory