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25067009: Autosomal variant form of transthyretin (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
42008017 Autosomal variant form of transthyretin en Synonym Active Case insensitive SNOMED CT core
755224015 Autosomal variant form of transthyretin (disorder) en Fully specified name Active Case insensitive SNOMED CT core


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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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