Related MeSH Hierarchy (8)
Diseases [C] » Neoplasms [C04] » Precancerous Conditions » Xeroderma Pigmentosum
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Xeroderma Pigmentosum
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Xeroderma Pigmentosum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Photosensitivity Disorders » Xeroderma Pigmentosum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Pigmentation Disorders » Xeroderma Pigmentosum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Xeroderma Pigmentosum
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Xeroderma Pigmentosum
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » DNA Repair-Deficiency Disorders » Xeroderma Pigmentosum
Description
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
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Phase 2 Indicated Drugs (1)
Phase 1 Indicated Drugs (2)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 2 Indications (3)
Organization Involved with Phase 1 Indications (2)
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UMLS Data
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