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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
10007381000172114 porteur d'une mutation génétique à risque élevé de cancer fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
10007391000172112 porteur d'une mutation génétique à haut risque de cancer fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
14645551000172119 porteur d'une mutation génétique à risque élevé de néoplasme malin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
14645561000172117 porteur d'une mutation génétique à haut risque de tumeur maligne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
3985481000172115 drager van genmutatie met hoog risico op maligne neoplasma nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
3985491000172117 drager van genmutatie met hoog risico op maligniteit nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of high risk cancer mutation gene (finding) Associated morphology Congenital anomaly 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

Reference Sets

Belgian subset for medical problems in patient health records

Description inactivation indicator reference set

GB English

US English

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