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Concept information

Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > Factor XI Deficiency
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Coagulation Protein Disorders > Factor XI Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > Factor XI Deficiency
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > Factor XI Deficiency

Terme préférentiel

Factor XI Deficiency  

Type

  • mesh:Descriptor

Définition

  • A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.

Concept générique

Concepts associés

Synonyme(s)

  • Deficiency, Factor 11
  • Deficiency, Factor Eleven
  • Deficiency, Factor XI
  • Factor 11 Deficiency
  • Factor Eleven Deficiency
  • Hemophilia C
  • Plasma Thromboplastin Antecedent Deficiency
  • Rosenthal's Syndrome
  • Rosenthal Syndrome

Qualificatif(s) autorisé(s)

Traductions

  • Déficit en facteur XI

    français

  • Carence en facteur XI
  • Déficit en FXI
  • Déficit en précurseur de thromboplastine plasmatique (PTA)
  • Hémophilie C
  • Syndrome de Rosenthal

URI

http://data.loterre.fr/ark:/67375/JVR-MX52RRQP-F

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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 02/05/2017