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Neoplasms > Precancerous Conditions > Xeroderma Pigmentosum
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Xeroderma Pigmentosum
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > 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
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

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Xeroderma Pigmentosum  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Kaposi Disease
  • Kaposi's Disease

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-XQDKJH0F-0

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