Congenital factor XI deficiency
ICD-10 Code
D68.1
Congenital factor XI deficiency
Definition
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.
Also known as congenital factor XI deficiency, factor XI deficiency, autosomal dominant, factor XI deficiency, autosomal recessive, haemophilia C, hemophilia C, hereditary Factor XI deficiency, hereditary factor XI deficiency disease, plasma thromboplastin antecedent deficiency, PTA deficiency, Rosenthal factor deficiency, Rosenthal syndrome, Rosenthal's disease — per MONDO