Any nonepidermolytic palmoplantar keratoderma in which the cause of the disease is a mutation in the KRT16 gene.
Comprehensive, easy-to-understand information about this condition
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hereditary painful callosities
MONDO:0007248
palmoplantar keratoderma-esophageal carcinoma syndrome
MONDO:0007856
focal palmoplantar and gingival keratoderma
MONDO:0007860
tyrosinemia type II
MONDO:0010160
hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
MONDO:0011884
nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
MONDO:0014460