Congenital Hypofibrinogenemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2584774
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Genes

6 genes associated with the disease Congenital Hypofibrinogenemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
FCGRT Fc fragment of IgG, receptor, transporter, alpha
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain