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205488003: Chondrodysplasia, otherwise specified (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315107014 Chondrodysplasia OS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2983297018 Chondrodysplasia, otherwise specified (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2983356010 Chondrodysplasia, otherwise specified en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Chondrodysplasia, otherwise specified Is a Mesomelic dysplasia false Inferred relationship Some
    Chondrodysplasia, otherwise specified Occurrence Congenital false Inferred relationship Some
    Chondrodysplasia, otherwise specified Finding site Skeletal system structure false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Associated morphology Dysplasia false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Finding site Bone structure false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Finding site Bone structure false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Chondrodysplasia, otherwise specified Occurrence Congenital false Inferred relationship Some 2
    Chondrodysplasia, otherwise specified Finding site Bone structure false Inferred relationship Some 2
    Chondrodysplasia, otherwise specified Associated morphology Congenital dysplasia false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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