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GTR Home > Conditions/Phenotypes > Hereditary factor X deficiency disease

Hereditary factor X deficiency disease

Synonyms
Congenital factor X deficiency; STUART-PROWER FACTOR DEFICIENCY
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

A rare inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms. [from ORDO]

Available tests

7 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (7 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: FX, FXA, F10
    Summary: coagulation factor X

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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