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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Keratoderma, Palmoplantar
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Keratoderma, Palmoplantar
Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Keratoderma, Palmoplantar

Preferred term

Keratoderma, Palmoplantar  

Type

  • Topical Descriptor

Broader concept

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Related concepts

Entry terms

  • Hyperkeratosis Palmaris et Plantaris
  • Keratoses, Palmoplantar
  • Keratosis Palmaris et Plantaris
  • Keratosis, Palmoplantar
  • Palmoplantar Keratoderma
  • Palmoplantar Keratoses
  • Palmoplantar Keratosis

Note

  • KERATODERMA, PALMOPLANTAR, DIFFUSE is also available; do not confuse entry term HYPERKERATOSIS PALMARIS ET PLANTARIS with POROKERATOSIS PALMARIS ET PLANTARIS DISSEMINATA see POROKERATOSIS

Scope note

  • Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis).

History note

  • 93; was KERATOSIS PALMARIS ET PLANTARIS 1974-92; KERATODERMA, PALMOPLANTAR was see KERATOSIS PALMARIS ET PLANTARIS 1990-92

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URI

http://www.yso.fi/onto/mesh/D007645

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