factor XIII deficiency hemorrhagic disease congenital hematological disorder congenital factor XIII deficiency https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/5537 https://www.malacards.org/card/congenital_factor_xiii_deficiency https://www.malacards.org/card/factor_xiii_deficiency SCTID:50189006 MONDO:0018029 UMLS:C0015530 fibrin stabilising factor deficiency Orphanet:331 fibrin-stabilizing factor deficiency Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. ICD9:286.3 MEDGEN:4639 DOID:2211 fibrin stabilizing factor deficiency NCIT:C131633 NANDO:2200681 GARD:0010766