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pachyonychia congenita 3
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any pachyonychia congenita in which the cause of the disease is a mutation in the KRT6A gene.
Uniprot Description An autosomal dominant genodermatosis characterized by hypertrophic nail dystrophy, painful and highly debilitating plantar keratoderma, oral leukokeratosis, and a variety of epidermal cysts.