Conditions / Genetic
hemophilia B
info · Genetic · ICD-10: D67
A hemophilia that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
Signs and symptoms
- Reduced factor IX activity
- Bruising susceptibility
- Persistent bleeding after trauma
- Joint hemorrhage
- Prolonged whole-blood clotting time
- Osteoarthritis
- Gastrointestinal hemorrhage
- Prolonged partial thromboplastin time
- Epistaxis
- Melena
Medications that may treat it
anti-inhibitor coagulant complex danaparoid dicumarol etranacogene dezaparvovec factor IX factor VII fidanacogene elaparvovec fitusiran marstacimab phenprocoumon warfarin
Also known as: Congenital factor IX deficiency; Congenital factor IX disorder; deficiency, functional factor IX; factor IX deficiency