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32160009: Congenital fiber type disproportion myopathy (disorder)

    Status: retired, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    485146017 Congenital fibre type disproportion myopathy en Synonym Active Case insensitive SNOMED CT core
    53727015 Congenital fiber type disproportion en Synonym Inactive Initial character case insensitive SNOMED CT core
    53728013 Congenital fiber type disproportion myopathy en Synonym Active Case insensitive SNOMED CT core
    763410017 Congenital fiber type disproportion myopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital fibre type disproportion myopathy Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
    Congenital fibre type disproportion myopathy Finding site Skeletal muscle system structure false Inferred relationship Some
    Congenital fibre type disproportion myopathy Associated morphology Congenital anomaly false Inferred relationship Some
    Congenital fibre type disproportion myopathy Occurrence Congenital false Inferred relationship Some
    Congenital fibre type disproportion myopathy Is a Congenital myopathy false Inferred relationship Some
    Congenital fibre type disproportion myopathy Finding site Skeletal muscle structure false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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