hereditary nonpolyposis colorectal cancer type 2 Disease Ontology Browser

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Disease Ontology Browser

hereditary nonpolyposis colorectal cancer type 2 (DOID:0070274)
Alliance: disease page
Synonyms: COCA2; familial nonpolyposis colon cancer type 2; FCC2; HNPCC2
Alt IDs: OMIM:609310
Definition: A Lynch syndrome that has_material_basis_in heterozygous mutation in the MLH1 gene on chromosome 3p22.2.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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