Sickle-cell trait

Preferred Label : Sickle-cell trait;

Inclusion CIM-10 : Heterozygous hemoglobin S; Hb-S trait;

Diag associé à un acte (%) : 65.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D573;

UMLS CUI

C0037054;

Automatic exact mappings (from CISMeF team)
- Hb-S trait [MedDRA LLT]
- Heterozygous hemoglobin S [MedDRA LLT]
Currated CISMeF NLP mapping
- Sickle Cell Trait [NCIt concept]
- Sickle cell trait [MedDRA Preferred Term]
- Sickle cell trait (disorder) [SNOMED CT concept]
- Sickle-cell trait [MedDRA LLT]
- sickle cell trait [MeSH Descriptor]
- sickle cell trait [SNOMED Notion]
- sickle cell trait [MeSH concept]
Orphanet concepts
- Hemoglobinopathy [ORDO Disease]
- Sickle cell disease and related diseases [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hb-S trait [MedDRA LLT]
- Hemoglobin S [LOINC component]
- Heterozygous haemoglobin S [MedDRA LLT]
- Heterozygous hemoglobin S [MedDRA LLT]
- Sickle Cell Trait [NCIt concept]
- Sickle cell trait [MedDRA Preferred Term]
- Sickle cell trait [ICD-11 Subcategory]
- Sickle cell trait (disorder) [SNOMED CT concept]
- Sickle-cell trait [MedDRA LLT]
- Sickle-cell trait [ICD-9 code]
- sickle cell trait [MeSH Descriptor]
- sickle cell trait [MeSH concept]
- sickle cell trait [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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