Hemoglobin Trait

Preferred Label : Hemoglobin Trait;

NCIt definition : A condition in which a person is heterozygous for a globin gene, with a one normal allele and one defective allele.;

Alternative definition : NICHD: A condition in which a person has a combination of normal and abnormal globin alleles with minimal or no clinical phenotype.;

Details

Origin ID

C95534;

UMLS CUI

C2987213;

Automatic exact mappings (from CISMeF team)
- Haemoglobin C trait [MedDRA Preferred Term]
- Haemoglobin D trait [MedDRA Preferred Term]
- Haemoglobin E trait [MedDRA Preferred Term]
- hemoglobin c trait [SNOMED Notion]
- hemoglobin d trait [SNOMED Notion]
- hemoglobin e trait [SNOMED Notion]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [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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