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
Related Concepts
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See Also
MeSH Record
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
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NLM Classification
WR 265
AMA Style
References
- National Library of Medicine. Xeroderma Pigmentosum. Medical Subject Headings (MeSH). 2026. Unique ID D014983. http://id.nlm.nih.gov/mesh/2026/D014983
- Xeroderma Pigmentosum. In: Wikipedia. https://en.wikipedia.org/wiki/Xeroderma_pigmentosum
- Xeroderma Pigmentosum. In: Wikidata. https://www.wikidata.org/wiki/Q612693