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18148005: Congenital 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
    30649010 Congenital myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
    745532019 Congenital 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 myopathy Is a Myopathy false Inferred relationship Existential restriction modifier
    Congenital myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Benign congenital hypotonia Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Myopathy with abnormality of histochemical fiber type Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Hereditary myositis ossificans Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Congenital hereditary muscular dystrophy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Congenital articular rigidity with myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Congenital fiber type disproportion myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Floppy infant syndrome Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Zebra body myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Central core disease Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Sarcotubular myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Congenital muscular hypertrophy-cerebral syndrome Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Multi-core congenital myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Mixed congenital myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Congenital myopathy with abnormal subcellular organelles Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Nemaline myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier
    Myotubular myopathy Is a False Congenital myopathy Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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