World Of Taxonomy
C84693Level 8

Epidermolytic Palmoplantar Keratoderma

**Semantic type:** Disease or Syndrome

**Definition:** A genetic skin disorder caused by mutations in the KRT9 gene. It is characterized by hyperkeratosis in the palms and soles resulting in abnormal thickening of the skin in these areas.

GET/api/v1/systems/nci_thesaurus/nodes/C84693
Official DownloadCC BY 4.0Source

Hierarchy Explorer

Loading...

Cross-system equivalences0

No cross-system equivalences mapped for this node.