Peutz-Jeghers syndrome (Q1544989)

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autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)
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English
Peutz-Jeghers syndrome
autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)
  • Colonic hamartomatous polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • gastric Peutz-Jeghers polyp
  • peutz-jeghers small bowel hamartoma
  • Peutz–Jeghers syndrome

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LD2D.0
Peutz-Jeghers syndrome
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Peutz-Jeghersin oireyhtymä
Peutz-Jeghers syndrom
Peutz-Jeghers syndrome
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