subungual hyperkeratosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A thickening of the stratum corneum in the region beneath the nails. (Human Phenotype Ontology, HP_0008392)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008392
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Genes

4 genes associated with the subungual hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CARD14 caspase recruitment domain family, member 14
KRT17 keratin 17, type I
MBTPS2 membrane-bound transcription factor peptidase, site 2
TRPV3 transient receptor potential cation channel, subfamily V, member 3