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698273002: Genetic short QT syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2973617016 Familial short QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2973622016 Genetic short QT syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2973624015 Genetic short QT syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Genetic short QT syndrome (disorder) est un(e) (attribut) Cardiac arrhythmia associated with genetic disorder (disorder) false Inferred relationship Some
    Genetic short QT syndrome (disorder) est un(e) (attribut) Short QT syndrome (disorder) false Inferred relationship Some
    Genetic short QT syndrome (disorder) localisation d'une constatation (attribut) cœur false Inferred relationship Some 1

    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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