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Descriptor English: Erythrokeratodermia Variabilis
Descriptor Spanish: Eritroqueratodermia Variable
Descriptor Portuguese: Eritroceratodermia Variável
Descriptor French: Érythrokératodermie variabilis
Entry term(s): Erythro et Keratodermia Variabilis
Erythrokeratodermia Figurata Variabilis
Erythrokeratodermia Figurata, Congenital Familial, in Plaques
Erythrokeratodermia Variabilis with Erythema Gyratum Repens
Erythrokeratodermia, Progressive Symmetric
Greither Disease
Mendes De Costa Syndrome
Progressive Symmetric Erythrokeratodermia
Transgrediens et Progrediens Palmoplantar Keratoderma
Tree number(s): C16.320.850.337
C17.800.229.606
C17.800.428.304
C17.800.827.337
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D056266
Scope note: An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Erythema (1998-2009)
Keratosis (2002-2009)
Skin Diseases, Genetic (2002-2009)
Public MeSH Note: 2010; ERYTHROKERATODERMIA FIGURATA, CONGENITAL FAMILIAL, IN PLAQUES and ERYTHROKERATODERMIA VARIABILIS WITH ERYTHEMA GYRATUM REPENS were indexed under PAPILLON-LEFEVRE DISEASE 2010-2016.
History Note: 2010
Related: Connexins MeSH
Keratoderma, Palmoplantar MeSH
DeCS ID: 53558
Unique ID: D056266
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2017/06/20
Erythrokeratodermia Variabilis - Preferred
Concept UI M0526847
Scope note An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA.
Preferred term Erythrokeratodermia Variabilis
Entry term(s) Erythro et Keratodermia Variabilis
Erythrokeratodermia Figurata Variabilis
Erythrokeratodermia Figurata, Congenital Familial, in Plaques
Erythrokeratodermia Variabilis with Erythema Gyratum Repens
Erythrokeratodermia, Progressive Symmetric
Mendes De Costa Syndrome
Progressive Symmetric Erythrokeratodermia
Greither Disease - Related but not broader or narrower
Concept UI M0527605
Preferred term Greither Disease
Entry term(s) Transgrediens et Progrediens Palmoplantar Keratoderma



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