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Concept information

disease > genetic disease > hereditary disease > peeling skin syndrome
disease > rare disease > peeling skin syndrome

Preferred term

peeling skin syndrome  

Definition(s)

  • Peeling skin syndrome (also known as "acral peeling skin syndrome", "continual peeling skin syndrome", "familial continual skin peeling", "idiopathic deciduous skin", and "keratolysis exfoliativa congenita") is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair.The acral form can be associated with TGM5. (Wikipedia)

Synonym(s)

  • continual skin peeling

In other languages

URI

http://data.loterre.fr/ark:/67375/VH8-KJJT05TH-D

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