Factor V Deficiency

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)

Also Known As:

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

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Hemorrhagic Disorders: 706
    - Factor V Deficiency: 222
  - Blood Coagulation Disorders: 168
    - Inherited Blood Coagulation Disorders: 76
      - Factor V Deficiency: 222
    - Coagulation Protein Disorders: 1
      - Factor V Deficiency: 222
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inherited Blood Coagulation Disorders: 76
    - Factor V Deficiency: 222

Madiha Ehtisham Selected Research

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Disease

Drug/Important Bio-Agent (IBA)