Term Name:	factor XIII deficiency
Synonyms:	deficiency, Laki-Lorand factor, Factor XIII deficiency disease, Hereditary factor XIII deficiency disease
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.
Ontology:	Human Disease [DOID:2211]   ( DOID:2211 )