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237971004: Hepatic glycogen phosphorylase deficiency (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    356669016 Hepatic glycogen phosphorylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
    356670015 Hers disease en Synonym Active Entire term case insensitive SNOMED CT core module
    356671016 Glycogen storage disease type VI en Synonym Active Only initial character case insensitive SNOMED CT core module
    626783017 Hepatic glycogen phosphorylase deficiency (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
    Hepatic glycogen phosphorylase deficiency Is a Glycogen storage disease false Inferred relationship Existential restriction modifier
    Hepatic glycogen phosphorylase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hepatic glycogen phosphorylase deficiency Finding site Liver structure false Inferred relationship Existential restriction modifier
    Hepatic glycogen phosphorylase deficiency Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
    Hepatic glycogen phosphorylase deficiency 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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