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25067009: autosomale variant van transthyretine (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
42008017 Autosomal variant form of transthyretin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
755224015 Autosomal variant form of transthyretin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7054361000146116 autosomale variant van transthyretine (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7054371000146110 autosomale variant van transthyretine nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal variant form of transthyretin Is a Metabolic disorder of transport true Inferred relationship Some
Autosomal variant form of transthyretin Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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