Neutropenia - CISMeF

Preferred Label : Neutropenia;

ICD-10 exclusion note : neutropenic splenomegaly (D73.81); transient neonatal neutropenia (P61.5);

Diag associé à un acte (%) : 60.2;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D70;

UMLS CUI

C0027947;

CISMeF manual mappings
- Granulocytopenic disorder (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- AGRANULOCYTOSIS [WHO-ART Preferred Term]
- Agranulocytic angina [MedDRA LLT]
- Agranulocytosis [PASCAL descriptor]
- Agranulocytosis [MedDRA Preferred Term]
- Agranulocytosis [HPO term]
- Agranulocytosis [ICD-10 category (who)]
- Agranulocytosis (disorder) [SNOMED CT concept]
- Angina agranulocytic [MedDRA LLT]
- GRANULOCYTOPENIA [WHO-ART High Level Term]
- Granulocytopenia [MedDRA Preferred Term]
- Granulocytopenia [NCIt concept]
- Granulocytopenia [PASCAL descriptor]
- Granulocytopenia [HPO term]
- agranulocytosis [MeSH Descriptor]
- agranulocytosis [MeSH concept]
- agranulocytosis [SNOMED Notion]
- agranulocytosis [Disease (Nov.)]
- agranulocytosis [DO Concept]
DO Cross reference
- agranulocytosis [DO Concept]
- neutropenia [DO Concept]
- severe congenital neutropenia [DO Concept]
Excluded by
- Other aplastic anemias and other bone marrow failure syndromes [ICD-10 category]
- Other disorders of white blood cells [ICD-10 category]
ICD-10 exclusion(s)
- Transient neonatal neutropenia [ICD-10 Sub-category]
Metaterm(s)
- hematology [CISMeF Metaterm]
Orphanet concepts
- Adult idiopathic neutropenia [ORDO Disease]
- Autosomal dominant severe congenital neutropenia [ORDO Disease]
- Autosomal recessive severe congenital neutropenia due to CSF3R deficiency [ORDO Disease]
- Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency [ORDO Disease]
- Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency [ORDO Disease]
- Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency [ORDO Disease]
- Congenital neutropenia-myelofibrosis-nephromegaly syndrome [ORDO Disease]
- Constitutional neutropenia [ORDO Disease]
- Cyclic neutropenia [ORDO Disease]
- Kostmann syndrome [ORDO Disease]
- Lichtenstein syndrome [ORDO Disease]
- Severe congenital neutropenia [ORDO Disease]
- X-linked severe congenital neutropenia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- NEUTROPENIA [WHO-ART Included Term]
- Neutropenia [MedDRA Preferred Term]
- Neutropenia [ICD-9 code]
- Neutropenia, unspecified [ICD-9 code]
- Neutropenias [MedDRA High Level Term]
- Neutropenic disorder (disorder) [SNOMED CT concept]
- neutropenia [MeSH Descriptor]
- neutropenia [MeSH concept]
- neutropenia [DO Concept]
- neutropenia, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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