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Keratosis palmoplantaris with periodontopathia and onychogryposis [Supplementary Concept]

Rare autosomal recessive disorder characterized by congenital PALMOPLANTAR KERATOSIS, flatfoot, onychogryphosis, PERIODONTITIS, ARACHNODACTYLY, and ACROOSTEOLYSIS.

Date introduced: August 25, 2010

MeSH Unique ID: C537627

Heading Mapped to:

Entry Terms:

  • Cochin Jewish disorder
  • Haim-Munk syndrome

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