Factor Viii Deficiency Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	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. (Human Disease Ontology, DOID_12134)
External Link	https://www.disgenet.org/browser/0/1/0/C3494187
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Genes

9 genes associated with the disease Factor Viii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
C6	complement component 6
COX8A	cytochrome c oxidase subunit VIIIA (ubiquitous)
F5	coagulation factor V (proaccelerin, labile factor)
F8	coagulation factor VIII, procoagulant component
F9	coagulation factor IX
LMAN1	lectin, mannose-binding, 1
MCFD2	multiple coagulation factor deficiency 2
SPRR2A	small proline-rich protein 2A
VWF	von Willebrand factor