| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A palmoplantar keratosis characterized by a well-demarcated, symmetric keratoderma located_in palms and located_in soles. (Human Disease Ontology, DOID_0050428) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007404 |
| Similar Terms | |
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1 genes associated with the nonepidermolytic palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KRT1 | keratin 1, type II |
