DO_rare_slim NCIthesaurus has material basis in has symptom disease has feature autosomal recessive disease blood coagulation disease factor XIII deficiency UMLS_CUI:C0015530 MIM:613235 SNOMEDCT_US_2025_09_01:50189006 GARD:10766 NCI:C98941 DOID:2211 MIM:613225 MESH:D005177 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. Factor XIII deficiency disease Hereditary factor XIII deficiency disease OMIM mapping confirmed by DO. [SN]. deficiency, Laki-Lorand factor disease_ontology hemarthrosis autosomal recessive inheritance bleeding epistaxis gum bleeding menorrhagia abnormal scar formation abnormal wound healing