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Summary Literature (0)
MIM:605258 - IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2

Xenbase Genes: aicda

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011528 - hyper-IgM syndrome type 2
MONDO:0015976 - obsolete hyper-IgM syndrome without susceptibility to opportunistic infections

Disease Ontology (DO):
DOID:0060758 - immunodeficiency with hyper-IgM type 2