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Summary Literature (0)
DOID:12259 - hemophilia B

Disease Ontology Definition:A 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.

Synonyms: Congenital factor IX deficiency, Congenital factor IX disorder, deficiency, functional factor IX, factor IX deficiency

Xenbase Genes : f9

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010604 - hemophilia B

MIM:
MIM:306900 - HEMOPHILIA B; HEMB

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): blood coagulation disease (is_a)