Search Ontology:
Human Disease

erythrokeratodermia variabilis

Term ID
DOID:0050467
Synonyms
  • Erythrokeratodermia Figurata Variabilis
  • Greither Disease
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
  • MESH:D056266
  • MIM:PS133200
  • NCI:C84696
  • ORDO:317
  • SNOMEDCT_US_2023_03_01:70041004
  • UMLS_CUI:C0265961
  • UMLS_CUI:C1851480
Ontology
Human Disease   ( DOID:0050467 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models
Citations