Marginal papular palmoplantar keratoderma
ORPHA:307995Acrokeratoelastoidosis of Costa
ORPHA:38Autosomal dominant diffuse mutilating palmoplantar keratoderma
ORPHA:307773Autosomal dominant palmoplantar keratoderma and congenital alopecia
ORPHA:1010Autosomal recessive palmoplantar keratoderma and congenital alopecia
ORPHA:1366Circumscribed palmoplantar hypokeratosis
ORPHA:69744Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
ORPHA:352662Diffuse palmoplantar keratoderma
ORPHA:307141Diffuse palmoplantar keratoderma-acrocyanosis syndrome
ORPHA:86918Disease with diffuse palmoplantar keratoderma as a major feature
ORPHA:307711Disease with focal palmoplantar keratoderma as a major feature
ORPHA:307871Disease with punctate palmoplantar keratoderma as a major feature
ORPHA:308023Focal acral hyperkeratosis
ORPHA:308013Focal palmoplantar and gingival keratoderma
ORPHA:2200Focal palmoplantar keratoderma
ORPHA:307837Haim-Munk syndrome
ORPHA:2342Hereditary painful callosities
ORPHA:79141Hereditary palmoplantar keratoderma
ORPHA:79357Hereditary palmoplantar keratoderma, Gamborg-Nielsen type
ORPHA:86923Huriez syndrome
ORPHA:384Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936Isolated diffuse palmoplantar keratoderma
ORPHA:307148Isolated focal palmoplantar keratoderma
ORPHA:307846Isolated punctate palmoplantar keratoderma
ORPHA:2338Mutilating palmoplantar keratoderma with periorificial keratotic plaques
ORPHA:659Naxos disease
ORPHA:34217Palmoplantar keratoderma-deafness syndrome
ORPHA:2202Palmoplantar keratoderma-esophageal carcinoma syndrome
ORPHA:2198Palmoplantar keratoderma-spastic paralysis syndrome
ORPHA:2201Palmoplantar keratoderma, Nagashima type
ORPHA:140966Palmoplantar porokeratosis of Mantoux
ORPHA:736Punctate palmoplantar keratoderma
ORPHA:307967Punctate palmoplantar keratoderma type 2
ORPHA:79502Skin fragility-woolly hair-palmoplantar keratoderma syndrome
ORPHA:293165Striate palmoplantar keratoderma
ORPHA:50942Woolly hair-palmoplantar keratoderma syndrome
ORPHA:420686