Diseases

Porphyria Cutanea Tarda

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.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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.

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MeSH Record

Aspects Covered

35 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

History Note

95; was PORPHYRIA, CUTANEA TARDA 1993-94

MeSH Record

Previous Indexing

  • Porphyria (1966-1992)

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References

  1. National Library of Medicine. Porphyria Cutanea Tarda. Medical Subject Headings (MeSH). 2026. Unique ID D017119. http://id.nlm.nih.gov/mesh/2026/D017119
  2. Porphyria Cutanea Tarda. In: Wikipedia. https://en.wikipedia.org/wiki/Porphyria_cutanea_tarda
  3. Porphyria Cutanea Tarda. In: Wikidata. https://www.wikidata.org/wiki/Q1479497