dystrophic toenail Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Toenail changes apart from changes of the color of the toenail (nail dyschromia) that involve partial or complete disruption of the various keratinous layers of the nail plate. (Human Phenotype Ontology, HP_0001810)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001810
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Genes

3 genes associated with the dystrophic toenail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NOTCH1 notch 1
RAB7A RAB7A, member RAS oncogene family
WNT10A wingless-type MMTV integration site family, member 10A