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721000146101: Hyalin myopathy (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2017. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

    Descriptions:

    Id Description Lang Type Status Case? Module
    6711000146116 Hyalin myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6721000146114 Hyalin myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hyalin myopathy Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
    Hyalin myopathy Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
    Hyalin myopathy Occurrence Congenital false Inferred relationship Some
    Hyalin myopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
    Hyalin myopathy Associated morphology Hyaline body false Inferred relationship Some 2
    Hyalin myopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
    Hyalin myopathy Is a Degenerative disorder false Inferred relationship Some
    Hyalin myopathy Finding site Skeletal muscle structure false Inferred relationship Some 3
    Hyalin myopathy Occurrence Congenital false Inferred relationship Some 3
    Hyalin myopathy Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

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