factor x activation deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced ability to transform factor X into its activated form factor Xa. (Human Phenotype Ontology, HP_0008354)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008354
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Genes

1 genes associated with the factor x activation deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO6 anoctamin 6