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240072005: Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    359672010 Benign scapuloperoneal muscular dystrophy with cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module
    359673017 Hauptmann-Thannhauser muscular dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
    629164019 Benign scapuloperoneal muscular dystrophy with cardiomyopathy (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
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Is a X-linked muscular dystrophy not predominantly limb girdle false Inferred relationship Existential restriction modifier
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Existential restriction modifier
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy 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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