factor VIII deficiency

Summary

DOID:12134 - factor VIII deficiency

Disease Ontology Definition:A hemophilia that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged.

Synonyms: classic hemophilia, Congenital factor VIII disorder, Subhemophilia, classic hemophilia A, Hemophilia A

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: f8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010602 - hemophilia A

MONDO:0010602 - hemophilia A

MIM:

MIM:306700 - HEMOPHILIA A; HEMA

MIM:306700 - HEMOPHILIA A; HEMA

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view

Parent(s): blood coagulation disease (is_a), hemophilia (is_a), X-linked monogenic disease (is_a), X-linked recessive disease (is_a)