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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, combined immunodeficiency, X-linked combined immunodeficiency

Xenbase Genes : cd3g, tap2, il7r, il2rg, tap1, tfrc, cd40lg, il21r, tapbp, ak2, prkdc, chd7, cd3e, b2m, bcl10, [+]

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

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

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

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