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epidermodysplasia verruciformis

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Epidermodysplasia verruciformis (EV) is a rare inherited genodermatosis characterized by chronic infection with human papillomavirus (HPV) leading to polymorphous cutaneous lesions and high risk of developing non melanoma skin cancer.
Uniprot Description Rare autosomal recessive genodermatosis associated with a high risk of skin carcinoma that results from an abnormal susceptibility to infection by specific human papillomaviruses. Infection leads to persistent wart-like or macular lesions.
Disease Ontology Description An autosomal recessive disease that results_in skin squamous cell carcinoma located_in skin, associated with a high risk of carcinoma. It is characterized by abnormal susceptibility to human papillomaviruses of the skin and has_symptom lesions on the body.
Mondo Term and Equivalent IDs
MONDO:0009176:  epidermodysplasia verruciformis
GARD:0006357: 
MESH:D004819: 
NCIT:C126877: 
OMIMPS:226400: 
Orphanet:302: 
SCTID:19138001: 
UMLS:C0014522: