palmoplantar cutis laxa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Loose, wrinkled skin of hands and feet. (Human Phenotype Ontology, HP_0007517)
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4 genes associated with the palmoplantar cutis laxa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
FGFR2 fibroblast growth factor receptor 2
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
ZNF469 zinc finger protein 469