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DOID:0070271 - Lynch syndrome 1
Disease Ontology Definition:A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.
Synonyms: FCC1, HNPCC1, familial nonpolyposis colon cancer type 1, hereditary nonpolyposis colorectal cancer type 1,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Lynch syndrome (is_a)