Search Ontology:
Human Disease

hereditary nonpolyposis colorectal cancer type 6

Term ID
DOID:0070273
Synonyms
  • HNPCC6
Definition
A Lynch syndrome that has_material_basis_in heterozygous mutation in the TGFBR2 gene on chromosome 3p22. https://www.ncbi.nlm.nih.gov/pubmed/9590282
References
Ontology
Human Disease   ( DOID:0070273 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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