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719986000: Autosomal dominant limb girdle muscular dystrophy type 1C (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    3318720013 Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
    3318721012 Autosomal dominant limb girdle muscular dystrophy type 1C en Synonym Active Only initial character case insensitive SNOMED CT core module
    3318722017 Limb girdle muscular dystrophy due to caveolin-3 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
    3318723010 Limb-girdle muscular dystrophy 1C caveolin myopathy en Synonym Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal dominant limb girdle muscular dystrophy type 1C Is a Autosomal dominant muscular dystrophy with limb girdle distribution false Inferred relationship Existential restriction modifier
    Autosomal dominant limb girdle muscular dystrophy type 1C Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1C Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
    Autosomal dominant limb girdle muscular dystrophy type 1C Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1C Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1C Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
    Autosomal dominant limb girdle muscular dystrophy type 1C Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1C Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1C Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1C Clinical course Progressive false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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