[An autosomal dominant hereditary syndrome characterized by a variety of hamartomas and neoplasms including verrucous skin lesions, fibromas of the oral cavity, facial trichilemmomas, hamartomatous colonic polyps, thyroid neoplasms, breast cancer, and dysplastic gangliocytomas of the cerebellum. —2004 ( NCI )]
UMLS (NCI) C0018553 Relation/PAR: hamartoma
multiple primary neoplasia
Familiar Neoplastic Syndrome