Combined immunodeficiency, unspecified

Preferred Label : Combined immunodeficiency, unspecified;

Inclusion CIM-10 : Severe combined immunodeficiency disorder [SCID] NOS;

Diag associé à un acte (%) : 48.9;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D819;

UMLS CUI

C2711630;

Currated CISMeF NLP mapping
- Combined immunity deficiency [ICD-9 code]
- Combined immunodeficiency [HPO term]
- Combined immunodeficiency [MedDRA Preferred Term]
- Combined immunodeficiency disease (disorder) [SNOMED CT concept]
- combined T cell and B cell immunodeficiency [DO Concept]
- combined immunodeficiency [Disease (Nov.)]
Orphanet concepts
- Combined T and B cell immunodeficiency [ORDO Disease]
- Combined immunodeficiency due to CARMIL2 deficiency [ORDO Disease]
- Severe combined immunodeficiency [ORDO Disease]
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]

Keyword's position in hierarchy(ies) :

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