Search Ontology:
Human Disease

hereditary nonpolyposis colorectal cancer type 2

Term ID
DOID:0070274
Synonyms
  • COCA2
  • familial nonpolyposis colon cancer type 2
  • FCC2
  • HNPCC2
Definition
A Lynch syndrome that has_material_basis_in heterozygous mutation in the MLH1 gene on chromosome 3p22.2. https://www.ncbi.nlm.nih.gov/pubmed/8128251
References
Ontology
Human Disease   ( DOID:0070274 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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