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37666005: Glycogen storage disease type X (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2023. 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
    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
    4512701000241110 glycogénose de type X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    4512701000241110 glycogénose de type X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    glycogénose de type X Is a Glycogen storage disease false Inferred relationship Existential restriction modifier (core metadata concept)
    glycogénose de type X Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept)
    glycogénose de type X Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    glycogénose de type X Finding site Liver structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    glycogénose de type X Is a Glycogen storage disease, hepatic form false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

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