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Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > Factor XI Deficiency
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > 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 > Coagulation Protein Disorders > Factor XI Deficiency

Preferred term

Factor XI Deficiency  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

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

Note

  • a blood coag disord

Scope note

  • 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.

History note

  • 1973(1966)

In other languages

  • hemofilia C

    Finnish

  • C-hemofilia
  • faktori XI:n puute
  • faktori XI:n puutos
  • faktorin XI puute
  • faktorin XI puutos
  • haemophilia C
  • hyytymistekijä XI:n puute
  • hyytymistekijä XI:n puutos
  • hyytymistekijän XI puute
  • hyytymistekijän XI puutos
  • PTA-puute
  • PTA-puutos
  • tekijä XI:n puute
  • tekijä XI:n puutos
  • tekijän XI puute
  • tekijän XI puutos
  • Faktor XI-brist

    Swedish

URI

http://www.yso.fi/onto/mesh/D005173

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