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718178006: Autosomal dominant limb girdle muscular dystrophy type 1B (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
    3311388014 Autosomal dominant limb girdle muscular dystrophy type 1B (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
    3311389018 Autosomal dominant limb girdle muscular dystrophy type 1B 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 1B Is a Autosomal recessive muscular dystrophy with limb girdle distribution false Inferred relationship Existential restriction modifier
    Autosomal dominant limb girdle muscular dystrophy type 1B Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1B Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1B Is a Autosomal dominant muscular dystrophy with limb girdle distribution false Inferred relationship Existential restriction modifier
    Autosomal dominant limb girdle muscular dystrophy type 1B Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1B Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1B Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant limb girdle muscular dystrophy type 1B Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Autosomal dominant limb girdle muscular dystrophy type 1B 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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