has characteristic has characteristic has material basis in germline mutation in F11 autosomal genetic disease hemorrhagic disease congenital hematological disorder congenital factor XI deficiency https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5537 https://github.com/monarch-initiative/mondo/issues/9097 https://rarediseases.info.nih.gov/diseases/9670/factor-xi-deficiency https://www.malacards.org/card/factor_xi_deficiency plasma thromboplastin antecedent deficiency hereditary factor XI deficiency disease factor XI deficiency, autosomal recessive SCTID:49762007 ICD9:286.2 MEDGEN:8770 Rosenthal factor deficiency hemophilia C Rosenthal's disease haemophilia C hereditary Factor XI deficiency DOID:2229 PTA deficiency Orphanet:329 ICD10CM:D68.1 NCIT:C84705 Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery. UMLS:C0015523 hereditary factor XI deficiency congenital factor XI deficiency factor XI deficiency, autosomal dominant MONDO:0012897 GARD:0009670 icd11.foundation:413739466 OMIM:612416 Rosenthal syndrome factor XI deficiency inherited inherited blood coagulation disorder