severe combined immunodeficiency

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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 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 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

: dclre1c, rag1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): combined T cell and B cell immunodeficiency (is_a)