Factor II Deficiency

Preferred Label : Factor II Deficiency;

Alternative definition : NICHD: A coagulation disorder characterized by the partial or complete absence of prothrombin (factor II) activity in the blood.;

Details

Origin ID

C131737;

UMLS CUI

C4722227;

Automatic exact mappings (from CISMeF team)
- Factor II deficiency [MedDRA Preferred Term]
- Factor II deficiency (disorder) [SNOMED CT concept]
- PROTHROMBIN TIME PROLONGED [WHO-ART Included Term]
- hypoprothrombinemias [MeSH Descriptor]
- prothrombin deficiency [DO Concept]
Currated CISMeF NLP mapping
- factor II deficiency [Blood Transfusion thesaurus concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Factor II deficiency [MedDRA Preferred Term]
- Prothrombin deficiency, congenital [OMIM Phenotype]
- hypoprothrombinemias [MeSH Descriptor]
- hypoprothrombinemias [MeSH concept]
- prothrombin deficiency [DO Concept]
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]
disease_mapped_to_gene
- F2 Gene [NCIt concept]
related_to_genetic_biomarker
- F2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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