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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:0015974 - severe combined immunodeficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee