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Concept information

disease > genetic disease > hereditary disease > Kindler syndrome
disease > rare disease > Kindler syndrome

Terme préférentiel

Kindler syndrome  

Définition

  • Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a rare congenital disease of the skin caused by a mutation in the KIND1 gene. (Wikipedia)

Synonyme(s)

  • Kindler poikiloderma

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-ZZBM5ZLH-8

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