Patchy Palmoplantar Keratoderma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A focal type of palmoplantar keratoderma in whichonly certain areas of the palms and soles are affected. (Human Phenotype Ontology, HP_0005588)
External Link https://www.disgenet.org/browser/0/1/0/C4021633
Similar Terms
Downloads & Tools

Genes

5 genes associated with the disease Patchy Palmoplantar Keratoderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DSP desmoplakin
GJA1 gap junction protein, alpha 1, 43kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
KDSR 3-ketodihydrosphingosine reductase