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Hereditary nonpolyposis colorectal cancer
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Autosomal dominant genetic condition associated with a high risk of cancer in the colon
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11
Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers
scientific article published on 10 January 2012
Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype
article
Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?
article
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome
scientific article published on 07 November 2019
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes
scientific article published on 03 October 2018
Survival from colorectal carcinoma in HNPCC families as compared to the general population in Lithuania--initial results
scientific article published on 07 July 2006
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours
scientific article published on 01 January 2003
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses
scientific article published on 23 April 2015
Cancer Risks for PMS2-Associated Lynch Syndrome
scientific article published on 30 August 2018
Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome
scientific article published on 01 February 2007
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Hereditary nonpolyposis colorectal cancer (HNPCC) is a hereditary predisposition to colon cancer.

Instance of
class of disease
Subclass of
autosomal dominant disease
Hereditary cancer syndrome
Colorectal cancer
Neoplasm
Syndrome
Disease
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