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: SCID, combined T and B cell inborn immunodeficiency
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : tap2, il2rg, tap1, tapbp, ak2, ada, dclre1c, foxn1, ciita, rfxap, rfxank, rag2, ada.2, rfx5, rag1
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD