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GTR Home > Conditions/Phenotypes > Congenital factor V deficiency

Congenital factor V deficiency

Synonyms
Hereditary factor V deficiency disease; LABILE FACTOR DEFICIENCY; OWREN PARAHEMOPHILIA; PARAHEMOPHILIA
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

Factor V deficiency is a rare autosomal recessive bleeding disorder with variable phenotypic expression (summary by van Wijk et al., 2001). [from OMIM]

Available tests

3 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (3 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: FVL, PCCF, RPRGL1, THPH2, F5
    Summary: coagulation factor V

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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