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

Preferred term

Factor XIII Deficiency  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Deficiencies, Factor 13
  • Deficiencies, Factor Thirteen
  • Deficiencies, Factor XIII
  • Deficiency, Factor 13
  • Deficiency, Factor Thirteen
  • Deficiency, Factor XIII
  • Factor 13 Deficiencies
  • Factor 13 Deficiency
  • Factor Thirteen Deficiencies
  • Factor Thirteen Deficiency
  • Factor XIII Deficiencies

Scope note

  • A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis.

History note

  • 73

In other languages

  • hyytymistekijä XIII:n puutos

    Finnish

  • faktori XIII:n puute
  • faktori XIII:n puutos
  • faktorin XIII puute
  • faktorin XIII puutos
  • fibriiniä stabiloivan tekijän puute
  • fibriiniä stabiloivan tekijän puutos
  • hyytymistekijä XIII:n puute
  • hyytymistekijän XIII puute
  • hyytymistekijän XIII puutos
  • tekijä XIII:n puute
  • tekijä XIII:n puutos
  • tekijän XIII puute
  • tekijän XIII puutos
  • Faktor XIII-brist

    Swedish

URI

http://www.yso.fi/onto/mesh/D005177

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