|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 genes associated with the skin erosion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.