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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
    315107014 Chondrodysplasia OS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    590862017 Chondrodysplasia OS (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2983297018 Chondrodysplasia, otherwise specified (disorder) en Fully specified name 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 Only initial character 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 OS (disorder) Is a Mesomelic dysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
    Chondrodysplasia OS (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Chondrodysplasia OS (disorder) Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Chondrodysplasia OS (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Chondrodysplasia OS (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Chondrodysplasia OS (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    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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