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Medical Subject Headings

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Sisällön kieli

Käsitteen tiedot

Neoplasms > Precancerous Conditions > Xeroderma Pigmentosum
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Xeroderma Pigmentosum
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Xeroderma Pigmentosum
Nutritional and Metabolic Diseases > Metabolic Diseases > DNA Repair-Deficiency Disorders > Xeroderma Pigmentosum
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Xeroderma Pigmentosum
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Xeroderma Pigmentosum
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Pigmentation Disorders > Xeroderma Pigmentosum
Skin and Connective Tissue Diseases > Skin Diseases > Pigmentation Disorders > Xeroderma Pigmentosum
Skin and Connective Tissue Diseases > Skin Diseases > Photosensitivity Disorders > Xeroderma Pigmentosum

Käytettävä termi

Xeroderma Pigmentosum  

Tyyppi

  • Topical Descriptor

Yläkäsite

Assosiatiiviset käsitteet

Ohjaustermit

  • Kaposi Disease
  • Kaposi's Disease
  • Kaposis Disease

Huomautus

  • 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

Käyttöhuomautus

  • 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.

Huomautus muutoshistoriasta

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

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D014983

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RDF/XML TURTLE JSON-LD Luotu 1.1.1999, viimeksi muokattu 11.4.2022