onycholysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Detachment of the nail from the nail bed. (Human Phenotype Ontology, HP_0001806)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001806
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Genes

9 genes associated with the onycholysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CDSN corneodesmosin
FZD6 frizzled class receptor 6
GJB6 gap junction protein, beta 6, 30kDa
KRT85 keratin 85, type II
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
UROD uroporphyrinogen decarboxylase
WNT10A wingless-type MMTV integration site family, member 10A