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

Preferred term

Factor X Deficiency  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Deficiencies, Factor 10
  • Deficiencies, Factor Ten
  • Deficiencies, Factor X
  • Deficiency, Factor 10
  • Deficiency, Factor Ten
  • Deficiency, Factor X
  • Deficiency, Stuart Prower
  • Deficiency, Stuart-Prower
  • Deficiency, Stuart Prower Factor
  • Deficiency, Stuart-Prower Factor
  • Factor 10 Deficiencies
  • Factor 10 Deficiency
  • Factor Ten Deficiencies
  • Factor Ten Deficiency
  • Factor X Deficiencies
  • Stuart Prower Deficiency
  • Stuart-Prower Deficiency
  • Stuart Prower Factor Deficiency
  • Stuart-Prower Factor Deficiency
  • Ten Deficiencies, Factor

Note

  • a blood coag disord

Scope note

  • Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.

History note

  • 91(75); was see under HYPOPROTHROMBINEMIAS 1975-90

In other languages

  • hyytymistekijä X:n puutos

    Finnish

  • faktori X:n puute
  • faktori X:n puutos
  • faktorin X puute
  • faktorin X puutos
  • hyytymistekijä X:n puute
  • hyytymistekijän X puute
  • hyytymistekijän X puutos
  • Stuart Powerin tekijän puute
  • Stuart Powerin tekijän puutos
  • tekijä X:n puute
  • tekijä X:n puutos
  • tekijän X puute
  • tekijän X puutos
  • Faktor X-brist

    Swedish

URI

http://www.yso.fi/onto/mesh/D005171

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