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DOID:0070274 - hereditary nonpolyposis colorectal cancer type 2
Disease Ontology Definition:A Lynch syndrome that has_material_basis_in heterozygous mutation in the MLH1 gene on chromosome 3p22.2.
Synonyms: COCA2, FCC2, HNPCC2, familial nonpolyposis colon cancer type 2,
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)