Congenital Combined Immunodeficiency

Preferred Label : Congenital Combined Immunodeficiency;

NCIt definition : A broad classification of inherited disorders presenting at birth that affect both the cell-mediated and humoral aspects of the immune response. Circulating numbers of B lymphocytes, T lymphocytes and NK cells are variable but where present do not function properly. Susceptibility to infection is the primary concern.;

Details

Origin ID

C27871;

UMLS CUI

C2711630;

DO Cross reference
- combined T cell and B cell immunodeficiency [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Combined immunity deficiency [ICD-9 code]
- Combined immunity deficiency [MedDRA LLT]
- Combined immunodeficiencies [ICD-10 category]
- Combined immunodeficiency [HPO term]
- Combined immunodeficiency [MedDRA Preferred Term]
- Combined immunodeficiency disease (disorder) [SNOMED CT concept]
- Combined immunodeficiency syndrome [MedDRA LLT]
- Combined immunodeficiency, unspecified [ICD-10 Sub-category]
- combined T cell and B cell immunodeficiency [DO Concept]
Validated automatic mappings to NTBT
- combined T cell and B cell immunodeficiency [DO Concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_has_associated_disease
- Autoimmune Lymphoproliferative Syndrome-Related Lymphoma [NCIt concept]
- EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency [NCIt concept]
- Lymphoproliferative Disease Associated with Primary Immune Disorder [NCIt concept]
- Recurrent EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency [NCIt concept]
- Refractory EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency [NCIt concept]

Keyword's position in hierarchy(ies) :

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