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460495004: Long QT syndrome with genetic marker (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

    Descriptions:

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

    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 Existential restriction modifier
    Long QT syndrome with genetic marker Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Long QT syndrome with genetic marker Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier
    Long QT syndrome with genetic marker Finding site Heart structure false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Romano-Ward syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Existential restriction modifier
    Jervell and Lange-Nielsen syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Existential restriction modifier
    Andersen Tawil syndrome Is a False Long QT syndrome with genetic marker Inferred relationship Existential restriction modifier
    Timothy syndrome type 1 Is a False Long QT syndrome with genetic marker Inferred relationship Existential restriction modifier
    Timothy syndrome type 2 Is a False Long QT syndrome with genetic marker Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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