|
DOID:0070273 - hereditary nonpolyposis colorectal cancer type 6
Disease Ontology Definition:A Lynch syndrome that has_material_basis_in heterozygous mutation in the TGFBR2 gene on chromosome 3p22.
Synonyms: HNPCC6,
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)