MeSH Browser

MeSH Heading: Keratoderma, Palmoplantar, Epidermolytic
Tree Number(s): C16.320.850.475.440.500; C17.800.428.435.440.500; C17.800.827.475.440.500
Unique ID: D053546
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D053546
Scope Note: An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9.
Entry Term(s): EPPK (Epidermolytic Palmoplantar Keratoderma); Epidermolytic Palmoplantar Keratoderma Vorner Type; Hyperkeratosis, Localized Epidermolytic; Keratoderma, Epidermolytic Palmoplantar; Keratosis of Greither; Palmoplantar Keratoderma, Epidermolytic; Thost-Unna Disease, Epidermolytic; Unna-Thost Disease, Epidermolytic
Previous Indexing: Keratoderma, Palmoplantar, Diffuse (1989-2006)
Public MeSH Note: 2007
History Note: 2007
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2015/06/18

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Keratoderma, Palmoplantar, Epidermolytic MeSH Descriptor Data 2024