Search Ontology:

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. (2)

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: combined immunodeficiency

combined immunodeficiency Show first 5 Terms
has subtype: CD40 ligand deficiency DNA ligase IV deficiency Good syndrome immunodeficiency 14 immunodeficiency 15A ... Show All 19 Terms

CD40 ligand deficiency DNA ligase IV deficiency Good syndrome immunodeficiency 14 immunodeficiency 15A immunodeficiency 16 immunodeficiency 23 immunodeficiency 36 immunodeficiency 37 immunodeficiency 40 immunodeficiency 46 immunodeficiency 53 immunodeficiency 56 immunodeficiency 58 immunodeficiency 60 immunodeficiency 70 leukocyte adhesion deficiency purine nucleoside phosphorylase deficiency X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models