Combined immunodeficiencies

Preferred Label : Combined immunodeficiencies;

ICD-10 exclusion note : autosomal recessive agammaglobulinemia (Swiss type) (D80.0);

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Do not code with : true;

Details

Origin ID

D81;

UMLS CUI

C2711630;

Automatic exact mappings (from CISMeF team)
- combined immunodeficiency [DO Concept]
Currated CISMeF NLP mapping
- Combined T and B cell immunodeficiency [ORDO Disease]
- Combined immune deficiency [PASCAL descriptor]
- Combined immunity deficiency [ICD-9 code]
- Combined immunity deficiency [MedDRA LLT]
- Combined immunodeficiencies [ICD-11 Subcategory]
- Combined immunodeficiency [HPO term]
- Combined immunodeficiency [MedDRA Preferred Term]
- Combined immunodeficiency disease (disorder) [SNOMED CT concept]
- Combined immunodeficiency syndrome [MedDRA LLT]
- combined T cell and B cell immunodeficiency [DO Concept]
- combined immunodeficiency [Disease (Nov.)]
DO Cross reference
- combined T cell and B cell immunodeficiency [DO Concept]
Excluded by
- Disorders of purine and pyrimidine metabolism [ICD-10 category]
ICD-10 exclusion(s)
- Hereditary hypogammaglobulinemia [ICD-10 Sub-category]
Metaterm(s)
- allergy and immunology [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Combined immunity deficiency [MedDRA LLT]
- Combined immunity deficiency [ICD-9 code]
- Combined immunodeficiency [MedDRA Preferred Term]
- Combined immunodeficiency [HPO term]
- Combined immunodeficiency disease (disorder) [SNOMED CT concept]
- Combined immunodeficiency syndrome [MedDRA LLT]
- Congenital Combined Immunodeficiency [NCIt concept]
- combined T cell and B cell immunodeficiency [DO Concept]
Validated automatic mappings to BTNT
- Severe combined immunodeficiencies [ICD-11 Sub-sub category]

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