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

Preferred term

Factor VII Deficiency  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Deficiencies, Factor 7
  • Deficiencies, Factor Seven
  • Deficiencies, Factor VII
  • Deficiency, Factor 7
  • Deficiency, Factor Seven
  • Deficiency, Factor VII
  • Factor 7 Deficiencies
  • Factor 7 Deficiency
  • Factor Seven Deficiencies
  • Factor Seven Deficiency
  • Factor VII Deficiencies
  • Hypoproconvertinemia
  • Hypoproconvertinemias

Scope note

  • An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.

History note

  • 85; was HYPOPROCONVERTINEMIA 1963-84

In other languages

  • hyytymistekijä VII:n puutos

    Finnish

  • faktori VII:n puute
  • faktori VII:n puutos
  • faktorin VII puute
  • faktorin VII puutos
  • hyytymistekijä VII:n puute
  • hyytymistekijän VII puute
  • hyytymistekijän VII puutos
  • prokonvertiinin puute
  • prokonvertiinin puutos
  • prokonvertiinipuute
  • prokonvertiinipuutos
  • tekijä VII:n puute
  • tekijä VII:n puutos
  • tekijän VII puute
  • tekijän VII puutos
  • Faktor VII-brist

    Swedish

URI

http://www.yso.fi/onto/mesh/D005168

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