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25067009: Autosomal variant form of transthyretin (disorder)


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

Descriptions:

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


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 Existential restriction modifier
Autosomal variant form of transthyretin Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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