| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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. (Human Disease Ontology, DOID_13777) |
| External Link | http://www.omim.org/entry/226400 |
| Similar Terms | |
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2 genes associated with the epidermodysplasia verruciformis phenotype from the curated OMIM Gene-Disease Associations dataset.
