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 (11)
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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory