MeSH Browser

MeSH Supplementary: Palmoplantar Keratoderma, Nonepidermolytic
Unique ID: C563422
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563422
Entry Term(s): Keratoderma, Nonepidermolytic Palmoplantar; NEPPK Nonepidermolytic Palmoplantar Keratoderma; Nonepidermolytic Palmoplantar Keratoderma
Registry Numbers: 0
Heading Mapped to: *Keratoderma, Palmoplantar, Diffuse
Frequency: 18
Note: Hereditary, autosomal dominant nonepidermolytic palmoplantar keratoderma that is caused by mutations in the KERATIN-1 (KRT1) gene. OMIM: 600962
Date of Entry: 2012/11/05
Revision Date: 2019/06/20

Palmoplantar Keratoderma, Nonepidermolytic MeSH Supplementary Concept Data 2025