skin erosion Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A discontinuity of the skin exhibiting incomplete loss of the epidermis, a lesion that is moist, circumscribed, and usually depressed. (Human Phenotype Ontology, HP_0200041)
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3 genes associated with the skin erosion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DSP desmoplakin
LMNA lamin A/C
ZMPSTE24 zinc metallopeptidase STE24