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Disease Ontology Browser
erythrokeratodermia variabilis (DOID:0050467)
Alliance: disease page
Synonyms: Erythrokeratodermia Figurata Variabilis; Greither Disease
Alt IDs: MESH:D056266, NCI:C84696, OMIM:PS133200, ORDO:317, UMLS_CUI:C0265961, UMLS_CUI:C1851480
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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory