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56096001: Facioscapulohumeral muscular dystrophy (disorder)

    Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    497510015 FSH - Facioscapulohumeral muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
    497511016 FMD - Facioscapulohumeral muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
    497512011 FSHD - Facioscapulohumeral muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
    794570010 Facioscapulohumeral muscular dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    93289013 Fascioscapulohumeral muscular dystrophy en Synonym Active Case insensitive SNOMED CT core
    93290016 Landouzy-Dejerine muscular dystrophy en Synonym Active Case sensitive SNOMED CT core
    93291017 Landouzy-Déjérine muscular dystrophy en Synonym Active Initial character case insensitive SNOMED CT core
    93292012 Facioscapulohumeral muscular dystrophy en Synonym Active Case insensitive SNOMED CT core
    93293019 Limb-girdle muscular dystrophy en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Facioscapulohumeral muscular dystrophy Occurrence Congenital false Inferred relationship Some
    Facioscapulohumeral muscular dystrophy Associated morphology Congenital anomaly false Inferred relationship Some
    Facioscapulohumeral muscular dystrophy Is a Autosomal dominant muscular dystrophy not predominantly limb girdle false Inferred relationship Some
    Facioscapulohumeral muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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