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Echinobase
Summary Literature (0)
DOID:12259 - hemophilia B

Disease Ontology 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.

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

Echinobase Genes :


OMIM:
MIM:306900 - hemophilia b; hemb

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

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