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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ichthyosis Vulgaris
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ichthyosis Vulgaris
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Ichthyosis > Ichthyosis Vulgaris
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ichthyosis > Ichthyosis Vulgaris
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ichthyosis > Ichthyosis Vulgaris
Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Ichthyosis > Ichthyosis Vulgaris

Preferred term

Ichthyosis Vulgaris  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Dominant Ichthyosis Vulgaris
  • Ichthyosis Simplex
  • Ichthyosis Simplices
  • Ichthyosis Vulgaris, Dominant

Note

  • do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

Scope note

  • Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.

History note

  • 91

In other languages

  • yleinen kalansuomutauti

    Finnish

  • ichthyosis congenita vulgaris
  • ichthyosis vulgaris
  • tavallinen iktyoosi
  • tavallinen kalansuomutauti
  • yleinen autosomaalinen kalansuomutauti
  • Fiskfjällssjuka

    Swedish

  • Ichthyosis vulgaris

URI

http://www.yso.fi/onto/mesh/D016112

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