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237971004: Hepatic glycogen phosphorylase deficiency (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    356669016 Hepatic glycogen phosphorylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    356670015 Hers disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    356671016 Glycogen storage disease type VI en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    626783017 Hepatic glycogen phosphorylase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    844651000052111 brist på leverglykogenfosforylas sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    brist på leverglykogenfosforylas Is a Glycogen storage disease false Inferred relationship Some
    brist på leverglykogenfosforylas Occurrence Congenital false Inferred relationship Some
    brist på leverglykogenfosforylas Finding site Liver structure false Inferred relationship Some
    brist på leverglykogenfosforylas Finding site Skeletal muscle structure false Inferred relationship Some
    brist på leverglykogenfosforylas Finding site Body system structure false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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