FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Lynch syndrome 1 ID (Ontology) DOID:0070271 (Human Disease)
Definition A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.
Also Known As "COCA1" ; "familial nonpolyposis colon cancer type 1" ; "FCC1" (for all, see Synonyms field below)
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 Genes
 Lynch syndrome 1       1
 for disease ribbon | Lynch syndrome 1       1
 model of | Lynch syndrome 1       1
Spanning Tree (Parents/Children)
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autosomal dominant disease__
syndrome____________________|
                            Lynch syndrome
                             |__Lynch syndrome 1  1 rec.
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Is a Lynch syndrome
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Synonyms
  • "COCA1" EXACT OMO:0003012
    "familial nonpolyposis colon cancer type 1" EXACT
    "FCC1" EXACT OMO:0003012
    "hereditary nonpolyposis colorectal cancer type 1" EXACT
    "HNPCC1" EXACT OMO:0003012
Secondary IDs
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MIM:120435
NCI:C6725
UMLS_CUI:C2936783