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205529007: Amyotrophica congenita (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315183011 Amyotrophica congenita en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    590911019 Amyotrophica congenita (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Amyotrophica congenita est un(e) (attribut) affection d'un muscle squelettique false Inferred relationship Some
    Amyotrophica congenita morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
    Amyotrophica congenita est un(e) (attribut) Congenital anomaly of skeletal muscle false Inferred relationship Some
    Amyotrophica congenita localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some
    Amyotrophica congenita survenue (attribut) congénital false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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