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90671000119109: 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
1865441000195118 portatore/portatrice di gene di mutazione ad alto rischio di cancro it 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
2380671000195118 Träger/Trägerin eines Hochrisiko-Krebsmutationsgens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of high risk cancer mutation gene (finding) Associated morphology anomalie congénitale false Inferred relationship Some
Carrier of high risk cancer mutation gene (finding) Is a Genetic disorder carrier true Inferred relationship Some
Carrier of high risk cancer mutation gene (finding) Interprets General clinical state true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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