90671000119109: Carrier of high risk cancer mutation gene (finding)

• SNOMED CT Concept\Clinical finding (finding)\Carrier of disorder\Genetic disorder carrier\Carrier of high risk cancer mutation gene (finding)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3433007011	Carrier of high risk cancer mutation gene (finding)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3433008018	Carrier of high risk cancer mutation gene	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3433007011	Carrier of high risk cancer mutation gene (finding)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3433007011	Carrier of high risk cancer mutation gene (finding)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3433008018	Carrier of high risk cancer mutation gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3433008018	Carrier of high risk cancer mutation gene	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
870421000195112	Träger / Trägerin eines Hochrisiko-Krebsmutationsgens	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770661000241119	porteur d'une mutation génétique à risque élevé de cancer	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770671000241110	porteur d'une mutation génétique à haut risque de cancer	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770681000241112	porteur d'une mutation génétique à risque élevé de néoplasme malin	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770691000241114	porteur d'une mutation génétique à haut risque de tumeur maligne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770661000241119	porteur d'une mutation génétique à risque élevé de cancer	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770671000241110	porteur d'une mutation génétique à haut risque de cancer	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770681000241112	porteur d'une mutation génétique à risque élevé de néoplasme malin	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5770691000241114	porteur d'une mutation génétique à haut risque de tumeur maligne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
870421000195112	Träger / Trägerin eines Hochrisiko-Krebsmutationsgens	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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