Hyppää sisältöön

Medical Subject Headings

Hae sanastosta

Sisällön kieli

Käsitteen tiedot

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Steroid Metabolism, Inborn Errors > Ichthyosis, X-Linked
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Steroid Metabolism, Inborn Errors > Ichthyosis, X-Linked
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
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
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

Käytettävä termi

Ichthyosis, X-Linked  

Tyyppi

  • Topical Descriptor

Yläkäsite

Assosiatiiviset käsitteet

Ohjaustermit

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

Huomautus

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

Käyttöhuomautus

  • 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.

Huomautus muutoshistoriasta

  • 91

Muunkieliset termit

URI

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

Lataa tämä käsite:

RDF/XML TURTLE JSON-LD Luotu 12.2.1990, viimeksi muokattu 25.6.2024