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460495004: Long QT syndrome with genetic marker (disorder)

    Status: retired, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2922800017 Long QT syndrome with genetic marker (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
    2922801018 Long QT syndrome with genetic marker en Synonym Active Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Long QT syndrome with genetic marker Is a Congenital long QT syndrome false Inferred relationship Some
    Long QT syndrome with genetic marker Occurrence Congenital false Inferred relationship Some 2
    Long QT syndrome with genetic marker Finding site Cardiac conducting system structure false Inferred relationship Some
    Long QT syndrome with genetic marker Finding site Structure of heart false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Romano-Ward syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Some
    Jervell and Lange-Nielsen syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Some
    Andersen Tawil syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Some
    Timothy syndrome type 1 Is a False Long QT syndrome with genetic marker Inferred relationship Some
    Timothy syndrome type 2 Is a False Long QT syndrome with genetic marker Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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