Skip to main content

Medical Subject Headings

Search from vocabulary

Content language

Concept information

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

Preferred term

Factor XII Deficiency  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Coagulation Factor 12 Deficiency
  • Deficiencies, Factor 12
  • Deficiencies, Factor Twelve
  • Deficiencies, Factor XII
  • Deficiency, Factor 12
  • Deficiency, Factor Twelve
  • Deficiency, Factor XII
  • Deficiency, Hageman Factor
  • Factor 12 Deficiencies
  • Factor 12 Deficiency
  • Factor Deficiency, Hageman
  • Factor Twelve Deficiencies
  • Factor Twelve Deficiency
  • Factor XII Deficiencies
  • Hageman Factor Deficiency
  • Hageman Trait

Note

  • a blood coag disord

Scope note

  • An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders and is marked by prolonged clotting time.

History note

  • 1978

In other languages

  • hyytymistekijä XII:n puutos

    Finnish

  • faktori XII:n puute
  • faktori XII:n puutos
  • faktorin XII puute
  • faktorin XII puutos
  • Hageman-tekijän puute
  • Hageman-tekijän puutos
  • hyytymistekijä XII:n puute
  • hyytymistekijän XII puute
  • hyytymistekijän XII puutos
  • tekijä XII:n puute
  • tekijä XII:n puutos
  • tekijän XII puute
  • tekijän XII puutos
  • Faktor XII-brist

    Swedish

URI

http://www.yso.fi/onto/mesh/D005175

Download this concept:

RDF/XML TURTLE JSON-LD Created 4/27/77, last modified 5/2/17