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GTR Home > Conditions/Phenotypes > Congenital factor VII deficiency

Congenital factor VII deficiency

Summary

A rare, genetic, congenital vitamin K-dependant coagulation factor deficiency disorder characterized by decreased levels or absence of coagulation factor VII (FVII), resulting in bleeding diathesis of variable severity. [from ORDO]

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: SPCA, F7
    Summary: coagulation factor VII

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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