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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Neoplastic Syndromes, Hereditary > Peutz-Jeghers Syndrome
Neoplasms > Neoplastic Syndromes, Hereditary > Peutz-Jeghers Syndrome
... > Pathological Conditions, Signs and Symptoms > Pathologic Processes > Pigmentation Disorders > Hyperpigmentation > Melanosis > Lentigo > Peutz-Jeghers Syndrome
... > Skin and Connective Tissue Diseases > Skin Diseases > Pigmentation Disorders > Hyperpigmentation > Melanosis > Lentigo > Peutz-Jeghers Syndrome
Digestive System Diseases > Gastrointestinal Diseases > Intestinal Diseases > Intestinal Polyposis > Peutz-Jeghers Syndrome

Término preferido

Peutz-Jeghers Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.

Concepto genérico

Etiquetas alternativas

  • Lentiginosis, Perioral
  • Periorificial Lentiginosis Syndrome
  • Peutz-Jeghers Polyposis
  • Peutz-Jegher's Syndrome
  • Polyposis, Hamartomatous Intestinal
  • Polyps-and-Spots Syndrome

En otras lenguas

  • Syndrome de Peutz-Jeghers

    francés

  • Lentiginose périorificielle avec polypose viscérale
  • Polypose hamartomateuse intestinale
  • Polypose intestinale - pigmentation cutanée
  • Syndrome de Peutz-Jeghers-Touraine

URI

http://data.loterre.fr/ark:/67375/JVR-WS2J0CKR-4

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