OBO ID: DOID:0050467 |
Term Name: | erythrokeratodermia variabilis | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A skin disease that is characterized by areas of sharply demarcated, brown hyperkeratosis and has_material_basis_in mutations in genes encoding for connexin channels proteins in the epidermis. https://en.wikipedia.org/wiki/Erythrokeratodermia_variabilis | ||
References: |
|
||
Ontology: | Human Disease ( DOID:0050467 ) |
OTHER erythrokeratodermia variabilis PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.