(Q2562598)

English

hemophilia B

An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.

  • haemophilia B
  • Congenital factor IX deficiency
  • Congenital factor IX disorder
  • Factor IX deficiency
  • Hemophilia B (disorder)
  • deficiency, functional factor IX
  • factor IX deficiency
  • Christmas disease

Statements

Identifiers

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3B11.0
Haemophilia B
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14194469-n
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