Hereditary hemolytic anemia, unspecified

Preferred Label : Hereditary hemolytic anemia, unspecified;

Imprécision du diag : 1;

Diag associé à un acte (%) : 67.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D589;

UMLS CUI

C0002881;

Automatic exact mappings (from CISMeF team)
- Hereditary hemolytic anemia, unspecified [MedDRA LLT]
Currated CISMeF NLP mapping
- Congenital haemolytic anaemia [MedDRA LLT]
- Congenital haemolytic anaemia NOS [MedDRA LLT]
- Congenital hemolytic anemia [HPO term]
- Congenital hemolytic anemia [MedDRA LLT]
- Congenital hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary Hemolytic Anemia [NCIt concept]
- Hereditary haemolytic anaemia [MedDRA Preferred Term]
- Hereditary haemolytic anaemia NOS [MedDRA LLT]
- Hereditary haemolytic anaemias [MedDRA LLT]
- Hereditary hemolytic anemia [MedDRA LLT]
- Hereditary hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary hemolytic anemia, unspecified [ICD-9 code]
- Hereditary hemolytic anemias [MedDRA LLT]
- Hereditary hemolytic anemias [ICD-9 code]
- anemia, hemolytic, congenital [MeSH concept]
- anemia, hemolytic, congenital [MeSH Descriptor]
- congenital hemolytic anemia [DO Concept]
- congenital hemolytic anemia [Disease (Nov.)]
- congenital hemolytic anemia, nos [SNOMED Notion]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]
DO Cross reference
- congenital hemolytic anemia [DO Concept]
Orphanet concepts
- Hemoglobinopathy [ORDO Disease]
See also inter- (CISMeF)
- congenital hemolytic anemia [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital haemolytic anaemia [MedDRA LLT]
- Congenital haemolytic anaemia [Bloc CIM-11]
- Congenital haemolytic anaemia NOS [MedDRA LLT]
- Congenital hemolytic anemia [MedDRA LLT]
- Congenital hemolytic anemia [HPO term]
- Congenital hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary Hemolytic Anemia [NCIt concept]
- Hereditary haemolytic anaemia [MedDRA Preferred Term]
- Hereditary haemolytic anaemia NOS [MedDRA LLT]
- Hereditary haemolytic anaemia, unspecified [MedDRA LLT]
- Hereditary haemolytic anaemias [MedDRA LLT]
- Hereditary hemolytic anemia [MedDRA LLT]
- Hereditary hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary hemolytic anemia, unspecified [MedDRA LLT]
- Hereditary hemolytic anemia, unspecified [ICD-9 code]
- Hereditary hemolytic anemias [MedDRA LLT]
- Hereditary hemolytic anemias [ICD-9 code]
- anemia, hemolytic, congenital [MeSH Descriptor]
- anemia, hemolytic, congenital [MeSH concept]
- congenital hemolytic anemia [DO Concept]
- congenital hemolytic anemia [Disease (Nov.)]
- congenital hemolytic anemia, nos [SNOMED Notion]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]

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