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18148005: Congenital myopathy (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    30649010 Congenital myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    745532019 Congenital myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital myopathy est un(e) (attribut) Myopathy (disorder) false Inferred relationship Some
    Congenital myopathy localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital articular rigidity with myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Congenital fiber type disproportion myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    syndrome du nourrisson mou (trouble) est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    myopathie à corps zébrés (trouble) est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    myopathie congénitale à "central cores" (trouble) est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Sarcotubular myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Congenital muscular hypertrophy-cerebral syndrome (disorder) est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Multi-core congenital myopathy (disorder) est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Mixed congenital myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Congenital myopathy with abnormal subcellular organelles est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Nemaline myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Myotubular myopathy est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    hypotonie congénitale bénigne est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Myopathy with abnormality of histochemical fibre type est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Hereditary myositis ossificans est un(e) (attribut) False Congenital myopathy Inferred relationship Some
    Congenital hereditary muscular dystrophy est un(e) (attribut) False Congenital myopathy Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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