 Erythrokeratodermia Variabilis
"Erythrokeratodermia Variabilis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D056266
|
| MeSH Number(s) |
C16.320.850.337 C17.800.229.606 C17.800.428.304 C17.800.827.337
|
| Concept/Terms |
Erythrokeratodermia Variabilis- Erythrokeratodermia Variabilis
- Mendes De Costa Syndrome
- Erythrokeratodermia Figurata, Congenital Familial, in Plaques
- Erythro et Keratodermia Variabilis
- Erythrokeratodermia, Progressive Symmetric
- Progressive Symmetric Erythrokeratodermia
- Erythrokeratodermia Variabilis with Erythema Gyratum Repens
- Erythrokeratodermia Figurata Variabilis
Greither Disease- Greither Disease
- Transgrediens et Progrediens Palmoplantar Keratoderma
|
Below are MeSH descriptors whose meaning is more general than "Erythrokeratodermia Variabilis".
Below are MeSH descriptors whose meaning is more specific than "Erythrokeratodermia Variabilis".
This graph shows the total number of publications written about "Erythrokeratodermia Variabilis" by people in this website by year, and whether "Erythrokeratodermia Variabilis" was a major or minor topic of these publications.
![]()
To see the data from this visualization as text, click here.
Below are the most recent publications written about "Erythrokeratodermia Variabilis" by people in Profiles.
-
Shah K, Ansar M, Mughal ZU, Khan FS, Ahmad W, Ferrara TM, Spritz RA. Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix. J Med Genet. 2017 03; 54(3):186-189.
|
Similar Concepts
![expand description]()
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|