Hereditary Hemolytic Anemia

Preferred Label : Hereditary Hemolytic Anemia;

NCIt synonyms : Congenital Hemolytic Anemia;

NCIt definition : A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.;

Alternative definition : NICHD: Hemolytic anemia for which the cause is an inherited disorder.;

Details

Origin ID

C34379;

UMLS CUI

C0002881;

Automatic exact mappings (from CISMeF team)
- Hereditary haemolytic anaemia, unspecified [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Congenital haemolytic anaemia [Bloc CIM-11]
- 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 haemolytic anaemia [ICD-11 Category]
- 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 anemia, unspecified [ICD-10 Sub-category]
- Hereditary hemolytic anemias [ICD-9 code]
- Hereditary hemolytic anemias [MedDRA LLT]
- 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]
False automatic mappings
- Congenital haemolytic anaemia NOS [MedDRA LLT]
- congenital hemolytic anemia, nos [SNOMED Notion]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
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 [HPO term]
- Congenital hemolytic anemia [MedDRA LLT]
- Congenital hemolytic anemia (disorder) [SNOMED CT 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 [MedDRA LLT]
- Hereditary hemolytic anemia, unspecified [ICD-10 Sub-category]
- 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]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_has_finding
- Hereditary Lesion [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]

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