Prekallikrein Deficiency

Preferred Label : Prekallikrein Deficiency;

NCIt definition : A condition characterized by the congenital or acquired deficiency of prekallikrein. This deficiency is usually not associated with bleeding. The congenital deficiency is very rare. Acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease.;

Details

Origin ID

C99022;

UMLS CUI

C0272339;

Currated CISMeF NLP mapping
- Prekallikrein deficiency [OMIM Phenotype]
- Prekallikrein deficiency (disorder) [SNOMED CT concept]
- prekallikrein deficiency [MeSH concept]
- prekallikrein deficiency [MeSH Supplementary Concept]
- prekallikrein deficiency [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital prekallikrein deficiency [ORDO Disease]
- Prekallikrein deficiency [OMIM Phenotype]
- Prekallikrein deficiency (disorder) [SNOMED CT concept]
- prekallikrein deficiency [SNOMED Notion]
- prekallikrein deficiency [MeSH Supplementary Concept]
- prekallikrein deficiency [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
related_to_genetic_biomarker
- KLKB1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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