Hereditary spherocytosis

Preferred Label : Hereditary spherocytosis;

Inclusion CIM-10 : Congenital (spherocytic) hemolytic icterus; Minkowski-Chauffard syndrome; Acholuric (familial) jaundice;

Diag associé à un acte (%) : 69.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D580;

UMLS CUI

C0037889;

Currated CISMeF NLP mapping
- ANAEMIA SPHEROCYTIC [WHO-ART Preferred Term]
- Anaemia spherocytic [MedDRA LLT]
- Anemia spherocytic [MedDRA LLT]
- Hereditary Spherocytosis [NCIt concept]
- Hereditary spherocytosis [MedDRA Preferred Term]
- Hereditary spherocytosis [ORDO Disease]
- Hereditary spherocytosis [ICD-9 code]
- Hereditary spherocytosis [ICD-10 Sub-category (who)]
- Hereditary spherocytosis [ICD-11 More detail]
- Hereditary spherocytosis (disorder) [SNOMED CT concept]
- Minkowski-Chauffard syndrome [MedDRA LLT]
- Spherocytic anaemia [MedDRA Preferred Term]
- Spherocytic anemia [MedDRA LLT]
- hereditary spherocytosis [Disease (Nov.)]
- hereditary spherocytosis [DO Concept]
- hereditary spherocytosis, nos [SNOMED Notion]
- spherocytosis, hereditary [MeSH concept]
- spherocytosis, hereditary [MeSH Descriptor]
DO Cross reference
- hereditary spherocytosis [DO Concept]
Orphanet concepts
- Hemoglobinopathy [ORDO Disease]
- Hereditary spherocytosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ANAEMIA SPHEROCYTIC [WHO-ART Preferred Term]
- Anaemia spherocytic [MedDRA LLT]
- Anemia spherocytic [MedDRA LLT]
- Hereditary Spherocytosis [NCIt concept]
- Hereditary spherocytosis [MedDRA Preferred Term]
- Hereditary spherocytosis [ICD-9 code]
- Hereditary spherocytosis [ORDO Disease]
- Hereditary spherocytosis [ICD-11 More detail]
- Hereditary spherocytosis (disorder) [SNOMED CT concept]
- Minkowski-Chauffard syndrome [MedDRA LLT]
- Spherocytic anaemia [MedDRA Preferred Term]
- Spherocytic anemia [MedDRA LLT]
- hereditary spherocytosis [DO Concept]
- hereditary spherocytosis [Disease (Nov.)]
- hereditary spherocytosis, nos [SNOMED Notion]
- spherocytosis, hereditary [MeSH Descriptor]
- spherocytosis, hereditary [MeSH concept]

Keyword's position in hierarchy(ies) :

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