abnormality of the intrinsic pathway Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of the intrinsic pathway (also known as the contact activation pathway) of the coagulation cascade. (Human Phenotype Ontology, HP_0010989)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0010989
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Genes

14 genes associated with the abnormality of the intrinsic pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ALG6	ALG6, alpha-1,3-glucosyltransferase
F11	coagulation factor XI
F12	coagulation factor XII (Hageman factor)
F8	coagulation factor VIII, procoagulant component
F9	coagulation factor IX
GGCX	gamma-glutamyl carboxylase
LMAN1	lectin, mannose-binding, 1
MCFD2	multiple coagulation factor deficiency 2
MGAT2	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
MPI	mannose phosphate isomerase
PMM2	phosphomannomutase 2
PTPN11	protein tyrosine phosphatase, non-receptor type 11
VKORC1	vitamin K epoxide reductase complex, subunit 1
VWF	von Willebrand factor