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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 Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
    Amyotrophica congenita Finding site Skeletal muscle structure false Inferred relationship Some
    Amyotrophica congenita Occurrence Congenital false Inferred relationship Some
    Amyotrophica congenita Is a Disorder of skeletal muscle false Inferred relationship Some
    Amyotrophica congenita Associated morphology Congenital anomaly false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

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