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237971004: Hepatic glycogen phosphorylase deficiency (disorder)

    Status: retired, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    356669016 Hepatic glycogen phosphorylase deficiency en Synonym Active Case insensitive SNOMED CT core
    356670015 Hers disease en Synonym Active Case insensitive SNOMED CT core
    356671016 Glycogen storage disease type VI en Synonym Active Initial character case insensitive SNOMED CT core
    626783017 Hepatic glycogen phosphorylase deficiency (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
    Hepatic glycogen phosphorylase deficiency Finding site Body system structure false Inferred relationship Some
    Hepatic glycogen phosphorylase deficiency Occurrence Congenital false Inferred relationship Some
    Hepatic glycogen phosphorylase deficiency Finding site Liver structure false Inferred relationship Some
    Hepatic glycogen phosphorylase deficiency Finding site Skeletal muscle structure false Inferred relationship Some
    Hepatic glycogen phosphorylase deficiency Is a Glycogen storage disease false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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