About   Help   FAQ
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_2006:286.1, ICD9CM:286.1, MESH:D002836, NCI:C26721, UMLS_CUI:C0008533
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.

Disease References using Mouse Models (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory