Structured Summary
Abstract
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.
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Synonyms
9 entry terms
- 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
- Transgrediens et Progrediens Palmoplantar Keratoderma
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2010
MeSH Record
Previous Indexing
- Erythema (1998-2009)
- Keratosis (2002-2009)
- Skin Diseases, Genetic (2002-2009)
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AMA Style
References
- National Library of Medicine. Erythrokeratodermia Variabilis. Medical Subject Headings (MeSH). 2026. Unique ID D056266. http://id.nlm.nih.gov/mesh/2026/D056266
- Erythrokeratodermia Variabilis. In: Wikipedia. https://en.wikipedia.org/wiki/Erythrokeratodermia_variabilis
- Erythrokeratodermia Variabilis. In: Wikidata. https://www.wikidata.org/wiki/Q3591493