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... > Digestive System Diseases > Gastrointestinal Diseases > Intestinal Diseases > Colonic Diseases > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
... > Digestive System Diseases > Gastrointestinal Diseases > Intestinal Diseases > Intestinal Neoplasms > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
... > Digestive System Diseases > Gastrointestinal Diseases > Gastrointestinal Neoplasms > Intestinal Neoplasms > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
... > Digestive System Diseases > Digestive System Neoplasms > Gastrointestinal Neoplasms > Intestinal Neoplasms > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
... > Neoplasms > Neoplasms by Site > Digestive System Neoplasms > Gastrointestinal Neoplasms > Intestinal Neoplasms > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
... > Digestive System Diseases > Gastrointestinal Diseases > Intestinal Diseases > Rectal Diseases > Colorectal Neoplasms > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Neoplastic Syndromes, Hereditary > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
Neoplasms > Neoplastic Syndromes, Hereditary > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II
Nutritional and Metabolic Diseases > Metabolic Diseases > DNA Repair-Deficiency Disorders > Colorectal Neoplasms, Hereditary Nonpolyposis > Lynch Syndrome II

Preferred term

Lynch Syndrome II  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Colon Cancer, Familial Nonpolyposis, Type 2
  • Colorectal Cancer, Hereditary Nonpolyposis, Type 2
  • Lynch cancer family syndrome 2
  • Lynch Cancer Family Syndrome II

Scope note

  • Hereditary nonpolyposis colorectal neoplasms associated with other malignancies, more commonly of ovarian or uterine origin. When also associated with SEBACEOUS GLAND NEOPLASMS, it is called MUIR-TORRE SYNDROME.

History note

  • 2009; use COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS 1992-2008

In other languages

URI

http://www.yso.fi/onto/mesh/D055847

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