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Concept information

Preferred term

Factor V Deficiency  

Type

  • Topical Descriptor

Entry terms

  • Deficiencies, Factor 5
  • Deficiencies, Factor Five
  • Deficiencies, Factor V
  • Deficiencies, Labile Factor
  • Deficiency, Factor 5
  • Deficiency, Factor Five
  • Deficiency, Factor V
  • Deficiency, Labile Factor
  • Disease, Owren
  • Disease, Owren's
  • Factor 5 Deficiencies
  • Factor 5 Deficiency
  • Factor Five Deficiencies
  • Factor Five Deficiency
  • Factor V Deficiencies
  • Labile Factor Deficiencies
  • Labile Factor Deficiency
  • Owren Disease
  • Owren Parahemophilia
  • Owren's Disease
  • Owrens Disease
  • Parahemophilia
  • Parahemophilia, Owren
  • Parahemophilias

Note

  • a blood coag disord

Scope note

  • A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed)

History note

  • 73(64); was see under HYPOPROTHROMBINEMIAS 1963-72

In other languages

  • Finnish

  • faktori V:n puute
  • faktori V:n puutos
  • faktorin V puute
  • faktorin V puutos
  • FV-puute
  • FV-puutos
  • hyytymistekijä V:n puute
  • hyytymistekijän V puute
  • hyytymistekijän V puutos
  • proakseleriinin puute
  • proakseleriinin puutos
  • proakseleriinipuute
  • proakseleriinipuutos
  • tekijä V:n puute
  • tekijä V:n puutos
  • tekijän V puute
  • tekijän V puutos
  • Swedish

URI

http://www.yso.fi/onto/mesh/D005166

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