Congenital haemolytic anaemia

ICD-11 code : L3-3A1;

Preferred Label : Congenital haemolytic anaemia;

ICD-11 definition : A disease caused by determinants arising in the antenatal period . This disease is characterised by low levels of red blood cells in the body due to abnormal destruction of the red blood cells. This disease may present with pallor, fatigue, or shortness of breath. Confirmation is by identification of low red blood cell count in a blood sample.;

ICD-11 synonym : Constitutional haemolytic anaemia;

ICD-11 "other" category code : 3A1Y;

Details

Origin ID

950429256;

UMLS CUI

C0002881;

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 [Disease (Nov.)]
- congenital hemolytic anemia [DO Concept]
- congenital hemolytic anemia, nos [SNOMED Notion]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]
ICD-10 Mapping
- Other hereditary hemolytic anemias [ICD-10 category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 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 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 [ICD-9 code]
- Hereditary hemolytic anemia, unspecified [ICD-10 Sub-category]
- Hereditary hemolytic anemia, unspecified [MedDRA LLT]
- Hereditary hemolytic anemias [ICD-9 code]
- Hereditary hemolytic anemias [MedDRA LLT]
- 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]
Validated automatic mappings to NTBT
- Other hereditary hemolytic anemias [ICD-10 category]

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