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Medical Subject Headings

Hae sanastosta

Sisällön kieli

Käsitteen tiedot

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

Käytettävä termi

Porphyrias, Hepatic  

Tyyppi

  • Topical Descriptor

Yläkäsite

Alakäsitteet

Ohjaustermit

  • Hepatic Porphyria
  • Porphyria, Hepatic

Huomautus

  • do not confuse with PORPHYRIA, ERYTHROHEPATIC

Käyttöhuomautus

  • A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues.

Huomautus muutoshistoriasta

  • 2005 (1993)

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D017094

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