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240072005: Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder)

    Status: retired, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    359672010 Benign scapuloperoneal muscular dystrophy with cardiomyopathy en Synonym Active Case insensitive SNOMED CT core
    359673017 Hauptmann-Thannhauser muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
    629164019 Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Pathological process Pathological developmental process false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Pathological process Pathological developmental process false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Clinical course Progressive false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Some
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Congenital anomaly false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Dystrophy false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Some 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology Developmental abnormality false Inferred relationship Some 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 3
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Is a X-linked muscular dystrophy not predominantly limb girdle false Inferred relationship Some
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence Congenital false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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