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Disease Ontology Browser
immunodeficiency with hyper-IgM type 4 (DOID:0060760)
Alliance: disease page
Synonyms: HIGM4; hyper-IgM syndrome type 4
Alt IDs: OMIM:608184, ICD10CM:D80.5, ORDO:101091, ORDO:183666
Definition: A hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory