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Erythrokeratodermia Variabilis MeSH Descriptor Data 2022


MeSH Heading
Erythrokeratodermia Variabilis
Tree Number(s)
C16.320.850.337
C17.800.229.606
C17.800.428.304
C17.800.827.337
Unique ID
D056266
RDF Unique Identifier
http://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.
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
Transgrediens et Progrediens Palmoplantar Keratoderma
Previous Indexing
Erythema (1998-2009)
Keratosis (2002-2009)
Skin Diseases, Genetic (2002-2009)
See Also
Connexins
Keratoderma, Palmoplantar
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
Date Established
2010/01/01
Date of Entry
2009/07/06
Revision Date
2017/06/20
Erythrokeratodermia Variabilis Preferred
Greither Disease Related
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