About   Help   FAQ
Disease Ontology Browser
factor VIII deficiency (DOID:12134)
Alliance: disease page
Synonyms: Congenital factor VIII disorder; Hemophilia A; Subhemophilia
Alt IDs: OMIM:134500, ICD10CM:D66, ICD9CM:286.0, MESH:D006467, NCI:C27146, UMLS_CUI:C0019069
Definition: An X-linked disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory