Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:627 - severe combined immunodeficiency

Disease Ontology Definition:A combined T cell and B cell immunodeficiency that is caused by a defect in infection-fighting immune cells resulting in individuals with non-functional immune systems.

Synonyms: combined T and B cell inborn immunodeficiency, SCID

Xenbase Genes : cd3g, tap2, il7r, il2rg, tap1, tapbp, ak2, prkdc, chd7, cd3e, b2m, ikbkb, ada, dclre1c, foxn1, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015974 - severe combined immunodeficiency


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): combined immunodeficiency (is_a), combined T cell and B cell immunodeficiency (is_a)