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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
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory