Sickle-cell/Hb-C disease

Preferred Label : Sickle-cell/Hb-C disease;

Inclusion CIM-10 : Hb-S/Hb-C disease; Hb-SC disease;

Diag associé à un acte (%) : 66.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D572;

UMLS CUI

C0019034;

Automatic exact mappings (from CISMeF team)
- Sickle cell Hb-C disease without crisis [ICD-11 More detail]
- Sickle cell-hemoglobin C disease syndrome [ORDO Disease]
- sickle cell anemia [DO Concept]
DO Cross reference
- sickle cell anemia [DO Concept]
Orphanet concepts
- Hemoglobinopathy [ORDO Disease]
- Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome [ORDO Disease]
- Sickle cell anemia [ORDO Disease]
- Sickle cell disease and related diseases [ORDO Disease]
- Sickle cell disease associated with another hemoglobin anomaly [ORDO Disease]
- Sickle cell-beta-thalassemia disease syndrome [ORDO Disease]
- Sickle cell-hemoglobin C disease syndrome [ORDO Disease]
- Sickle cell-hemoglobin D disease syndrome [ORDO Disease]
- Sickle cell-hemoglobin E disease syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Haemoglobin SC disease [MedDRA LLT]
- Hb-SC [MedDRA LLT]
- Hemoglobin SC disease [LOINC component]
- Hemoglobin SC disease [MedDRA LLT]
- Sickle Cell-Hemoglobin C Disease [NCIt concept]
- Sickle cell Hb-C disease [MedDRA LLT]
- Sickle cell-hemoglobin C disease (disorder) [SNOMED CT concept]
- Sickle cell-hemoglobin C disease syndrome [ORDO Disease]
- Sickle-cell/Hb-C disease without crisis [ICD-9 code]
- hemoglobin SC disease [MeSH Descriptor]
- hemoglobin SC disease [MeSH concept]
- hemoglobin SC disease [Disease (Nov.)]
- sickle cell-hemoglobin c disease [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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