MeSH Browser

MeSH Supplementary: Keratosis palmoplantaris with periodontopathia and onychogryposis
Unique ID: C537627
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537627
Entry Term(s): Cochin Jewish disorder; Haim-Munk syndrome
Heading Mapped to: *Papillon-Lefevre Disease; *Acro-Osteolysis
Frequency: 4
Note: Rare autosomal recessive disorder characterized by congenital PALMOPLANTAR KERATOSIS, flatfoot, onychogryphosis, PERIODONTITIS, ARACHNODACTYLY, and ACROOSTEOLYSIS.
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Keratosis palmoplantaris with periodontopathia and onychogryposis MeSH Supplementary Concept Data 2024