Definition

A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor.

Synonyms

deficiency, Laki-Lorand factor
Factor XIII deficiency disease

Cross References

Parent Terms

Child Terms

None

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factor XIII deficiency

factor XIII deficiency

Associated Genes

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