Hemolytic Anemia due to Membrane Defect

Preferred Label : Hemolytic Anemia due to Membrane Defect;

NCIt related terms : Hemolytic Anemia due to Erythrocyte Membrane Defect; Anemia due to Membrane Defect;

NCIt definition : A group of inherited hemolytic anemias caused by erythrocyte membrane defects. This includes hereditary pyropoikilocytosis, hereditary spherocytosis and hereditary elliptocytosis.;

Alternative definition : NICHD: A group of inherited hemolytic anemias caused by erythrocyte membrane defects. This includes hereditary pyropoikilocytosis, hereditary spherocytosis, and hereditary elliptocytosis.;

Details

Origin ID

C101218;

UMLS CUI

C0272031;

Currated CISMeF NLP mapping
- Anemia due to membrane defect (disorder) [SNOMED CT concept]
- anemia due to membrane defect, nos [SNOMED Notion]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anemia due to membrane defect (disorder) [SNOMED CT concept]
- anemia due to membrane defect, nos [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network 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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