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