FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary nonpolyposis colorectal cancer type 2 ID (Ontology) DOID:0070274 (Human Disease)
Definition A Lynch syndrome that has_material_basis_in heterozygous mutation in the MLH1 gene on chromosome 3p22.2.
Also Known As "COCA2" ; "familial nonpolyposis colon cancer type 2" ; "FCC2" (for all, see Synonyms field below)
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 Genes
 hereditary nonpolyposis colorectal cancer type 2       1
 for disease ribbon | hereditary nonpolyposis colorectal cancer type 2       1
 model of | hereditary nonpolyposis colorectal cancer type 2       1
Spanning Tree (Parents/Children)
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autosomal dominant disease__
syndrome____________________|
                            Lynch syndrome
                             |__hereditary nonpolyposis colorectal cancer type 2  1 rec.
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Synonyms
  • "COCA2" EXACT OMO:0003012
    "familial nonpolyposis colon cancer type 2" EXACT
    "FCC2" EXACT OMO:0003012
    "HNPCC2" EXACT OMO:0003012
Secondary IDs
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MIM:609310