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52794005: 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
    87841011 Myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    87845019 Myopathic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    87846018 Myopathic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    790842010 Myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    87841011 Myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    87841011 Myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    87845019 Myopathic syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    87845019 Myopathic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    87846018 Myopathic disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    87846018 Myopathic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    790842010 Myopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    790842010 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
    Myopathy Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Proximal myopathy (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy in myasthenia gravis Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital myotonic dystrophy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Mitochondrial myopathy (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Triglyceride storage disease with ichthyosis Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Fingerprint myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Metabolic myopathy (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Débré-Sémélaigne's syndrome Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Paramyotonia congenita Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Reducing-body myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Oculocraniosomatic syndrome Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary myopathy associated with hydrocephalus Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy of extraocular muscles Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital myotonia, autosomal dominant form Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Secondary myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Luft's hypermetabolic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Amyotonia congenita (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary hollow viscus myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Toxic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myoclonus epilepsy AND ragged red fibers Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Muscular dystrophy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Megaconial myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Minimal change myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Eosinophilic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Ophthalmoplegia plus syndrome (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Isaacs syndrome (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myotonia acquisita Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myotonia levior Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    myopathie inflammatoire symptomatique associée à un autre trouble Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy due to disseminated lupus erythematosus Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy due to polyarteritis nodosa Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy due to rheumatoid arthritis Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy due to scleroderma Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Myopathy due to Sjögren's disease (disorder) Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    Symptomatic inflammatory myopathy in disease NOS Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    [X]Other specified myopathies Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    [X]Myopathy in infectious and parasitic diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    [X]Myopathy in endocrine diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    [X]Myopathy in other diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)
    [X]Inflammatory myopathy, not elsewhere classified Is a False Myopathy Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

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