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Human Disease

combined T cell and B cell immunodeficiency

Term ID
DOID:628
Synonyms
  • Congenital Combined Immunodeficiency
Definition
A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity. (3)
References
  • ICD10CM:D81
  • ICD9CM:279.2
  • NCI:C27871
  • ORDO:101972
  • SNOMEDCT_US_2023_03_01:442459007
  • UMLS_CUI:C2711630
Ontology
Human Disease   ( DOID:628 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models