Hereditary Persistence of Fetal Hemoglobin

Preferred Label : Hereditary Persistence of Fetal Hemoglobin;

NCIt definition : The persistence of substantial fetal hemoglobin production into adulthood, usually associated with hemoglobinopathies due to mutations in the alpha and/or beta chain of hemoglobin.;

Détails

Origin ID

C129072;

UMLS CUI

C0019025;

Automatic exact mappings (from CISMeF team)
- Hereditary persistence of fetal haemoglobin [ICD-11 Subcategory]
- Hereditary persistence of fetal hemoglobin [PASCAL descriptor]
- Hereditary persistence of fetal hemoglobin [MedDRA LLT]
- Hereditary persistence of fetal hemoglobin (disorder) [SNOMED CT concept]
- Hereditary persistence of fetal hemoglobin thalassemia (disorder) [SNOMED CT concept]
- beta-Thalassemia [MeSH Descriptor]
- hereditary persistence of fetal hemoglobin thalassemia, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary persistence of fetal haemoglobin [ICD-11 Subcategory]
- Hereditary persistence of fetal hemoglobin [PASCAL descriptor]
- Hereditary persistence of fetal hemoglobin [MedDRA LLT]
- Hereditary persistence of fetal hemoglobin (disorder) [SNOMED CT concept]
- Hereditary persistence of fetal hemoglobin [HPFH] [ICD-10 Sub-category]
- Hereditary persistence of foetal haemoglobin [MedDRA Preferred Term]
- hemoglobin F disease [MeSH concept]
- hereditary persistence of fetal hemoglobin [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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