Search Ontology:
Human Disease

Lynch syndrome 1

Term ID
DOID:0070271
Synonyms
  • familial nonpolyposis colon cancer type 1
  • FCC1
  • hereditary nonpolyposis colorectal cancer type 1
  • HNPCC1
Definition
A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16. (2)
References
Ontology
Human Disease   ( DOID:0070271 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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