716318002: Lynch syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Genetic disease\Hereditary disease\...
• \Hereditary neoplastic syndrome\Lynch syndrome
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Lynch syndrome

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3305504010	Lynch syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3305505011	Lynch syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3533539017	Patients and families with a germline mutation in one of the DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2) or the EPCAM gene but who have not met the criteria for hereditary nonpolyposis colon cancer.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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