combined T cell and B cell immunodeficiency

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: 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

MONDO:0015131 - combined immunodeficiency

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)