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:
- Haim-Munk syndrome
- Cochin Jewish disorder