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Disease Ontology Browser
combined T cell and B cell immunodeficiency (DOID:628)
Alliance: disease page
Synonyms: combined immunodeficiency; Congenital Combined Immunodeficiency
Alt IDs: ICD10CM:D81, ICD9CM:279.2, NCI:C27871, OMIM:PS300755, ORDO:101972, UMLS_CUI:C2711630
Definition: A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity.

Disease References using Mouse Models (9)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/18/2022
MGI 6.17
The Jackson Laboratory