Factor V Deficiency

Clinical Features

Phenotypes and symptoms related to Factor V Deficiency

  • Bruising susceptibility
  • Abnormal bleeding
  • Epistaxis
  • Abnormality of the coagulation cascade
  • Menorrhagia
  • Prolonged bleeding time
  • Prolonged partial thromboplastin time
  • Prolonged prothrombin time
  • Prolonged whole-blood clotting time
  • Reduced coagulation factor V activity

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Factor V Deficiency Is also known as owren parahemophilia, parahemophilia, labile factor deficiency.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Factor V Deficiency Recommended genes panels

Panel Name, Specifity and genes Tested/covered
F5.

By Molecular Diagnostic Laboratory University of Alberta (Canada).

F5
Specificity
100 %
Genes
100 %
Factor V Leiden Mutation Panel.

By Baylor Miraca Genetics Laboratories (United States).

F5
Specificity
100 %
Genes
100 %
Thrombophilia Mutation Panel.

By Baylor Miraca Genetics Laboratories (United States).

F2, F5, MTHFR
Specificity
34 %
Genes
100 %
Factor V Leiden.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

F5
Specificity
100 %
Genes
100 %
Factor V Leiden.

By Center for Human Genetics, Inc (United States).

F5
Specificity
100 %
Genes
100 %
Factor V Leiden Thrombophilia.

By Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital (United States).

F5
Specificity
100 %
Genes
100 %
Factor V Analysis.

By Molecular Pathology Laboratory University of Pennsylvania Health System (United States).

F5
Specificity
100 %
Genes
100 %
Factore V Leiden.

By Molecular Genetics Laboratory Centro de Investigaciones Endocrinologicas "Dr. Cesar Bergada" (Argentina).

F5
Specificity
100 %
Genes
100 %

You can get up to 99 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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