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Summary Literature (0)
DOID:628 - combined T cell and B cell immunodeficiency


Disease Ontology Definition:A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity.

Synonyms: Congenital Combined Immunodeficiency, X-linked combined immunodeficiency, combined immunodeficiency

Xenbase Genes : cd3g, tap2, il7r, il2rg, tap1, tfrc, cd40lg, tapbp, ak2, chd7, cd3e, b2m, ikbkb, ada, dclre1c, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015131 - congenital combined immunodeficiency

OMIM:
OMIM:312863 - COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): combined immunodeficiency (is_a), primary immunodeficiency disease (is_a)