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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Neoplastic Syndromes, Hereditary > Hamartoma Syndrome, Multiple
Neoplasms > Neoplastic Syndromes, Hereditary > Hamartoma Syndrome, Multiple
Neoplasms > Neoplasms, Multiple Primary > Hamartoma Syndrome, Multiple
Neoplasms > Hamartoma > Hamartoma Syndrome, Multiple

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Hamartoma Syndrome, Multiple  

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Tipo

  • mesh:Descriptor

Definición

  • A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • Cowden Disease
  • Cowden Syndrome
  • Cowden's Disease
  • Cowden's Syndrome
  • Multiple Hamartoma Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-C36W05W6-N

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RDF/XML TURTLE JSON-LD Creado 23/6/86, última modificación 29/6/18