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nevus, epidermal
Disease Summary
Associated Targets (6)
Tclin
4
Tchem
2
Mondo Description A benign, pigmented skin growth caused by an overgrowth of the epidermis. It is typically seen at birth, but can develop in early childhood or later in life. Most cases are sporadic, but familial patterns of inheritance have been observed.
Uniprot Description Epidermal nevi of the common, non-organoid and non-epidermolytic type are benign skin lesions and may vary in their extent from a single (usually linear) lesion to widespread and systematized involvement. They may be present at birth or develop early during childhood.
Disease Ontology Description A skin disease characterized by localized epidermal thickening with hyperpigmentation that develops at or shortly after birth.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0111162
GARD:0013025
MESH:C580062
NCIT:C4088
OMIM:162900
MONDO:0008093
High level summary of knowledge for a disease, including descriptions and datasource references.