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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, MESH:C564277, NCI:C564277, ORDO:101091, UMLS_CUI:C1842413
Definition: A hyper IgM syndrome that is 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 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
12/10/2024
MGI 6.24 		The Jackson Laboratory