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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C6725> ?p ?o ?g. }

• NCIT_C6725 IAO_0000115 "A rare genetic neoplastic syndrome with an autosomal dominant pattern of inheritance but incomplete penetrance. It is associated with a greater than 70 % risk of developing colorectal carcinoma. It is caused by a mutation in one of the mismatch repair genes: MSH2, MLH1, MSH6 or PMS2. It usually manifests at age 50 or younger with multiple synchronous or metachronous colorectal carcinomas. Clinical course is rapidly progressive. Prognosis is variable with a high risk for the development of additional colorectal carcinomas. However, survival is significantly better than non-HNPCC carcinomas of equivalent stage." @default.
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• NCIT_C6725 NCIT_NHC0 "C6725" @default.
• NCIT_C6725 NCIT_P106 "Disease or Syndrome" @default.
• NCIT_C6725 NCIT_P108 "Lynch 1 Syndrome" @default.
• NCIT_C6725 NCIT_P207 "C2674962" @default.
• NCIT_C6725 NCIT_P366 "Hereditary_Non-Polyposis_Colon_Cancer_Type_1" @default.
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