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DOID:0060760 - immunodeficiency with hyper-IgM type 4
Disease Ontology 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.
Synonyms: HIGM4, hyper-IgM syndrome type 4,
Xenbase Genes :
MONDO:0011985 - hyper-IgM syndrome type 4 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hyperimmunoglobulin syndrome (is_a)