GTR Home > Conditions/Phenotypes > Factor XIII subunit B deficiency

Summary

Factor XIII deficiency is an autosomal recessive hematologic disorder characterized by increased bleeding and poor wound healing. Most cases of congenital factor XIII deficiency result from mutation in the A subunit (Kangsadalampai et al., 1999). Ichinose et al. (1996, 2000) proposed a classification of factor XIII deficiency: XIIIA deficiency (formerly 'type II' F13 deficiency) and XIIIB deficiency (formerly 'type I' F13 deficiency), as well as a possible combined deficiency of the 2. [from OMIM]

Available tests

13 tests are in the database for this condition.

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  • Also known as: FXIIIB, F13B
    Summary: coagulation factor XIII B chain

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