hemophilia B

created [InstanceEdit:9670828] Shamovsky, Veronica, 2019-12-17
databaseName DOID
dbId 9670882
definition 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.
displayName hemophilia B
identifier 12259
name
  • hemophilia B
referenceDatabase [ReferenceDatabase:1247631] DOID
schemaClass Disease
synonym
  • factor IX deficiency
  • Congenital factor IX deficiency
  • deficiency, functional factor IX
  • Congenital factor IX disorder
url https://www.ebi.ac.uk/ols/ontologies/doid/terms?obo_id=DOID:12259

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