OBO ID: DOID:0070271
Term Name: Lynch syndrome 1 Search Ontology:
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)
OTHER Lynch syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MSH2 Colorectal cancer, hereditary nonpolyposis, type 1 120435
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None