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37666005: Glycogen storage disease type X (disorder)


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
62830011 Glycogen storage disease type X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62831010 GSD X en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
62833013 Glycogenosis due to inactive phosphorylase AND kinase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769559012 Glycogen storage disease type X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease type X est un(e) (attribut) maladie de stockage du glycogène (trouble) false Inferred relationship Some
Glycogen storage disease type X est un(e) (attribut) Glycogen storage disease, hepatic form true Inferred relationship Some
Glycogen storage disease type X localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some
Glycogen storage disease type X survenue (attribut) congénital true Inferred relationship Some 1
Glycogen storage disease type X localisation d'une constatation (attribut) foie true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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