Keratoderma, Palmoplantar

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).

推出的年份: 1993

树号: C16.320.850.475, C17.800.428.435, C17.800.827.475

MeSH 单一 ID: D007645

进入的组:

Keratodermas, Palmoplantar
Palmoplantar Keratodermas
Keratosis Palmaris et Plantaris
Palmoplantar Keratoderma
Hyperkeratosis Palmaris et Plantaris
Keratosis, Palmoplantar
Keratoses, Palmoplantar
Palmoplantar Keratoses
Palmoplantar Keratosis
Meleda Disease
Disease, Meleda
Keratosis Palmoplantaris Transgradiens of Siemens
Mal de Meleda
Meleda, Mal de
de Meleda, Mal

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Skin Diseases, Genetic [C16.320.850]

All MeSH Categories
- Diseases Category
  - Skin and Connective Tissue Diseases [C17]
    - Skin Diseases [C17.800]
      - Keratosis [C17.800.428]

All MeSH Categories
- Diseases Category
  - Skin and Connective Tissue Diseases [C17]
    - Skin Diseases [C17.800]
      - Skin Diseases, Genetic [C17.800.827]

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Keratoderma, Palmoplantar

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