|  Help  |  About  |  Contact Us

DO Term : Lynch syndrome [DOID:3883] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.
  • synonyms:
  • PS120435,
  • Hereditary nonpolyposis colorectal cancer syndrome,
  • DOID:3040,
  • ORDO:144,
  • Hereditary non-polyposis colon cancer,
  • Hereditary nonpolyposis colon cancer syndrome,
  • hereditary nonpolyposis colorectal neoplasm,
  • GARD:9905,
  • MESH:D003123,
  • UMLS_CUI:C4552100,
  • DOID:0050586,
  • Hereditary non-polyposis colorectal cancer syndrome,
  • SNOMEDCT_US_2023_03_01:700064004,
  • Hereditary Defective Mismatch Repair syndrome,
  • Hereditary non-polyposis colorectal cancer,
  • HNPCC,
  • OMIM:PS120435,
  • hereditary nonpolyposis colorectal cancer,
  • Hereditary non-polyposis colon cancer syndrome,
  • Hereditary nonpolyposis colon cancer,
  • NCI:C8494,
  • UMLS_CUI:C0009405
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents