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Medical Subject Headings

Hae sanastosta

Sisällön kieli

Käsitteen tiedot

Digestive System Diseases > Liver Diseases > Porphyrias, Hepatic > Porphyria Cutanea Tarda
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Porphyrias, Hepatic > Porphyria Cutanea Tarda
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Porphyrias, Hepatic > Porphyria Cutanea Tarda
Nutritional and Metabolic Diseases > Metabolic Diseases > Porphyrias > Porphyrias, Hepatic > Porphyria Cutanea Tarda

Käytettävä termi

Porphyria Cutanea Tarda  

Tyyppi

  • Topical Descriptor

Yläkäsite

Käyttöhuomautus

  • An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.

Huomautus muutoshistoriasta

  • 95; was PORPHYRIA, CUTANEA TARDA 1993-94

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D017119

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RDF/XML TURTLE JSON-LD Luotu 22.5.1992, viimeksi muokattu 11.4.2022