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205488003: Chondrodysplasia, otherwise specified (disorder)

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

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