Condition: Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome


rs587777737 in GRHL2 gene and Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome PMID 25152456 2014 Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome.