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111507009: Becker muscular dystrophy (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    178749014 Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363278014 Becker's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363279018 Muscular dystrophy - cardiac type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363280015 Obscure cardiomyopathy of Africa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363281016 Restrictive cardiomyopathy with endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363282011 Idiopathic mural endomyocardial disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363283018 Endomyocardial sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363284012 African endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363285013 BMD - Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363286014 Endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    632282019 Becker muscular dystrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    178749014 Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363278014 Becker's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363279018 Muscular dystrophy - cardiac type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363279018 Muscular dystrophy - cardiac type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363280015 Obscure cardiomyopathy of Africa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363281016 Restrictive cardiomyopathy with endomyocardial fibrosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363281016 Restrictive cardiomyopathy with endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363282011 Idiopathic mural endomyocardial disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363282011 Idiopathic mural endomyocardial disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363283018 Endomyocardial sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363283018 Endomyocardial sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    363284012 African endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363285013 BMD - Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    363286014 Endomyocardial fibrosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    363286014 Endomyocardial fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    632282019 Becker muscular dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    632282019 Becker muscular dystrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Becker muscular dystrophy Is a Primary restrictive cardiomyopathy false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Is a affection spécifique du muscle cardiaque false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Is a X-linked muscular dystrophy with abnormal dystrophin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Finding site Myocardium structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Is a Structural disorder of heart false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Becker muscular dystrophy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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