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Disease Ontology Browser
hemophilia B (DOID:12259)
Alliance: disease page
Synonyms: Congenital factor IX deficiency; Congenital factor IX disorder; deficiency, functional factor IX; factor IX deficiency
Alt IDs: OMIM:306900, ICD10CM:D67, ICD9CM:286.1, MESH:D002836, NCI:C26721, UMLS_CUI:C0008533
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.

Disease References using Mouse Models (8)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory