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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ichthyosis, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ichthyosis, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Ichthyosis, X-Linked
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ichthyosis > Ichthyosis, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ichthyosis > Ichthyosis, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Ichthyosis > Ichthyosis, X-Linked
Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Ichthyosis > Ichthyosis, X-Linked
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Steroid Metabolism, Inborn Errors > Ichthyosis, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Steroid Metabolism, Inborn Errors > Ichthyosis, X-Linked

Preferred term

Ichthyosis, X-Linked  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Ichthyoses, Sex-Linked
  • Ichthyosis, Sex Linked
  • Ichthyosis, Sex-Linked

Note

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

Scope note

  • Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is characterized by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.

History note

  • 91

In other languages

URI

http://www.yso.fi/onto/mesh/D016114

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