Genetic anomalies of leukocytes

Preferred Label : Genetic anomalies of leukocytes;

Inclusion CIM-10 : Hereditary leukomelanopathy; May-Hegglin syndrome; Alder syndrome; Hereditary leukocytic hyposegmentation; Alder (granulation) (granulocyte) anomaly; Pelger-Huët (granulation) (granulocyte) anomaly; Pelger-Huët syndrome; Hereditary leukocytic hypersegmentation; May-Hegglin (granulation) (granulocyte) anomaly;

ICD-10 exclusion note : Chédiak (-Steinbrinck)-Higashi syndrome (E70.330);

Diag associé à un acte (%) : 75.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D720;

UMLS CUI

C0017377;

Automatic exact mappings (from CISMeF team)
- Alder-Reilly anomaly [ICD-11 More detail]
- Alders syndrome (disorder) [SNOMED CT concept]
- Chédiak-Higashi syndrome (disorder) [SNOMED CT concept]
- Genetic anomalies of leukocytes [ICD-9 code]
Currated CISMeF NLP mapping
- Congenital Leukocyte Abnormality [NCIt concept]
- Genetic anomalies of leucocytes [MedDRA LLT]
- Genetic anomalies of leukocytes [MedDRA LLT]
- Genetic anomaly of leukocyte (disorder) [SNOMED CT concept]
- genetic anomaly of leukocyte, nos [SNOMED Notion]
ICD-10 exclusion(s)
- Albinism [ICD-10 Sub-category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Leukocyte Abnormality [NCIt concept]
- Constitutional disorders of neutrophil function [ICD-11 Subcategory]
- Constitutional neutrophilia [ICD-11 Sub-sub category]
- Genetic anomalies of leucocytes [MedDRA LLT]
- Genetic anomalies of leukocytes [MedDRA LLT]
- Genetic anomalies of leukocytes [ICD-9 code]
- Genetic anomaly of leukocyte (disorder) [SNOMED CT concept]
- genetic anomaly of leukocyte, nos [SNOMED Notion]

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