DOID:627 - severe combined immunodeficiency
Disease Ontology Definition:A combined T cell and B cell immunodeficiency that is caused by a defect in several genes encoding for B and T lymphocytes resulting in individuals with non-functional immune systems.
Synonyms: SCID, combined T and B cell inborn immunodeficiency,
Echinobase Genes : dclre1c, rag1
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee