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52794005: Myopathy (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    87841011 Myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
    87842016 Myopathy, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    87843014 Myopathic syndrome, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    87844015 Myopathic disease, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    87845019 Myopathic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    87846018 Myopathic disease en Synonym Active Entire term case insensitive SNOMED CT core module
    790842010 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
    Myopathy Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier
    Myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Proximal myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy in myasthenia gravis Is a False Myopathy Inferred relationship Existential restriction modifier
    Congenital myotonic dystrophy Is a False Myopathy Inferred relationship Existential restriction modifier
    Mitochondrial myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Congenital myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Triglyceride storage disease with ichthyosis Is a False Myopathy Inferred relationship Existential restriction modifier
    Fingerprint myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Metabolic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Débré-Sémélaigne's syndrome Is a False Myopathy Inferred relationship Existential restriction modifier
    Paramyotonia congenita Is a False Myopathy Inferred relationship Existential restriction modifier
    Reducing-body myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Oculocraniosomatic syndrome Is a False Myopathy Inferred relationship Existential restriction modifier
    Hereditary myopathy associated with hydrocephalus Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy of extraocular muscles Is a False Myopathy Inferred relationship Existential restriction modifier
    Congenital myotonia, autosomal dominant form Is a False Myopathy Inferred relationship Existential restriction modifier
    Secondary myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Luft's hypermetabolic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Amyotonia congenita Is a False Myopathy Inferred relationship Existential restriction modifier
    Hereditary hollow viscus myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Toxic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Myoclonus epilepsy AND ragged red fibers Is a False Myopathy Inferred relationship Existential restriction modifier
    Muscular dystrophy Is a False Myopathy Inferred relationship Existential restriction modifier
    Megaconial myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Minimal change myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Eosinophilic myopathy Is a False Myopathy Inferred relationship Existential restriction modifier
    Ophthalmoplegia plus syndrome Is a False Myopathy Inferred relationship Existential restriction modifier
    Isaacs syndrome Is a False Myopathy Inferred relationship Existential restriction modifier
    Myotonia acquisita Is a False Myopathy Inferred relationship Existential restriction modifier
    Myotonia levior Is a False Myopathy Inferred relationship Existential restriction modifier
    Symptomatic inflammatory myopathy associated with another disorder Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy due to disseminated lupus erythematosus Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy due to polyarteritis nodosa Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy due to rheumatoid arthritis Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy due to scleroderma Is a False Myopathy Inferred relationship Existential restriction modifier
    Myopathy due to Sjögren's disease Is a False Myopathy Inferred relationship Existential restriction modifier
    Symptomatic inflammatory myopathy in disease NOS Is a False Myopathy Inferred relationship Existential restriction modifier
    [X]Other specified myopathies Is a False Myopathy Inferred relationship Existential restriction modifier
    [X]Myopathy in infectious and parasitic diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier
    [X]Myopathy in endocrine diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier
    [X]Myopathy in other diseases classified elsewhere Is a False Myopathy Inferred relationship Existential restriction modifier
    [X]Inflammatory myopathy, not elsewhere classified Is a False Myopathy Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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