Diseases

Xeroderma Pigmentosum

A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.

MeSH Record

Classification

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See Also

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Synonyms

3 entry terms
  • Kaposi Disease
  • Kaposi's Disease
  • Kaposis Disease

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

Indexing Annotation

if non-neoplastic, coordinate IM with precoordinated organ/disease term (IM); if neoplastic, coordinate IM with organ/neoplasm term (IM); do not confuse KAPOSI DISEASE with SARCOMA, KAPOSI

MeSH Record

History Note

63; KAPOSI DISEASE was KAPOSI'S DISEASE 1963-97

MeSH Hierarchy

Tree Numbers

MeSH Record

NLM Classification

WR 265

AMA Style

References

  1. National Library of Medicine. Xeroderma Pigmentosum. Medical Subject Headings (MeSH). 2026. Unique ID D014983. http://id.nlm.nih.gov/mesh/2026/D014983
  2. Xeroderma Pigmentosum. In: Wikipedia. https://en.wikipedia.org/wiki/Xeroderma_pigmentosum
  3. Xeroderma Pigmentosum. In: Wikidata. https://www.wikidata.org/wiki/Q612693