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32160009: Congenital fiber type disproportion myopathy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

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