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Metadata
ID DOID:0070271
Name Lynch syndrome 1
Definition A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.
https://www.ncbi.nlm.nih.gov/pubmed/8261515, https://www.ncbi.nlm.nih.gov/pubmed/8574961
Xrefs

OMIM:120435

Synonyms

familial nonpolyposis colon cancer type 1 [EXACT]

FCC1 [EXACT]

hereditary nonpolyposis colorectal cancer type 1 [EXACT]

HNPCC1 [EXACT]

Parent Relationships

is_a Lynch syndrome

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