blurred vision Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Lack of sharpness of vision resulting in the inability to see fine detail. (Human Phenotype Ontology, HP_0000622)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000622
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Genes

6 genes associated with the blurred vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ATP1A2	ATPase, Na+/K+ transporting, alpha 2 polypeptide
COL4A1	collagen, type IV, alpha 1
KCNA1	potassium channel, voltage gated shaker related subfamily A, member 1
MAPT	microtubule-associated protein tau
SCN9A	sodium channel, voltage gated, type IX alpha subunit
TACSTD2	tumor-associated calcium signal transducer 2