Isolated punctate palmoplantar keratoderma
ORPHA:2338Acrokeratoelastoidosis of Costa
ORPHA:38Autosomal dominant diffuse mutilating palmoplantar keratoderma
ORPHA:307773Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
ORPHA:308031Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
ORPHA:308041Carvajal syndrome
ORPHA:65282Circumscribed palmoplantar hypokeratosis
ORPHA:69744Diffuse 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:384Hypopigmentation-punctate palmoplantar keratoderma syndrome
ORPHA:324561Isolated diffuse palmoplantar keratoderma
ORPHA:307148Isolated focal non-epidermolytic palmoplantar keratoderma
ORPHA:448264Isolated focal palmoplantar keratoderma
ORPHA:307846Marginal papular palmoplantar keratoderma
ORPHA:307995Naxos 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 1
ORPHA:79501Punctate palmoplantar keratoderma type 2
ORPHA:79502Skin fragility-woolly hair-palmoplantar keratoderma syndrome
ORPHA:293165Striate palmoplantar keratoderma
ORPHA:50942Woolly hair-palmoplantar keratoderma syndrome
ORPHA:420686