About: Lynch Syndrome

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Lynch Syndrome
equivalentClass	nodeID://b633578
Semantic_Type	Neoplastic Process
Preferred_Name	Lynch Syndrome
UMLS_CUI	C0009405
ALT_DEFINITION	An inherited disorder in which affected individuals have a higher-than-normal chance of developing colorectal cancer and certain other types of cancer, often before the age of 50.NCI-GLOSS
Neoplastic_Status	Malignant
Legacy_Concept_Name	Hereditary_Non-Polyposis_Colon_Cancer
FULL_SYN	hereditary nonpolyposis colon cancerPTNCI-GLOSSCDR0000044884 Hereditary Nonpolyposis Colorectal NeoplasmSYNCI Familial Non-Polyposis Colon Cancer (hMSH2, hMLH1, hPMS1, hPMS2)SYNCI HNPCCPTNCI-GLOSSCDR0000044410 Hereditary Defective Mismatch Repair SyndromeSYNCI Lynch SyndromePTNCI Hereditary Nonpolyposis Colon CancerSYNCI Hereditary Non-Polyposis Colon Cancer (hMSH2, hMLH1, hPMS1, hPMS2)SYNCI Hereditary Non-Polyposis Colon CancerSYNCI HNPCCABNCI Lynch syndromePTNCI-GLOSSCDR0000044882 Hereditary Colorectal Endometrial Cancer SyndromeSYNCI
DEFINITION	An autosomal dominant hereditary neoplastic syndrome characterized by the development of colorectal carcinoma and a high risk of developing endometrial carcinoma, gastric carcinoma, ovarian carcinoma, renal pelvis carcinoma, and small intestinal carcinoma. Patients often develop colorectal carcinomas at an early age (mean, 45 years). In the majority of the cases the lesions arise from the proximal colon. At the molecular level, high-frequency microsatellite instability is present.NCI
code	C8494
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