FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server  |   User: [n/a]

254057007: Omodysplasia II (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module Reference Sets
    378203019 Omodysplasia II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core Description inactivation indicator reference set: Concept non-current
    378204013 Omodysplasia, Borochowitz type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core Description inactivation indicator reference set: Concept non-current
    644896018 Omodysplasia II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core Description inactivation indicator reference set: Concept non-current
    2023411000052114 omodysplasi 2 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    omodysplasi 2 Is a Atelosteogenesis false Inferred relationship Some
    omodysplasi 2 Finding site Bone structure false Inferred relationship Some 1
    omodysplasi 2 Occurrence Congenital false Inferred relationship Some
    omodysplasi 2 Finding site Skeletal system structure false Inferred relationship Some 1
    omodysplasi 2 Associated morphology Dysplasia false Inferred relationship Some 1
    omodysplasi 2 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    omodysplasi 2 Associated morphology medfödd missbildning false Inferred relationship Some
    omodysplasi 2 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    omodysplasi 2 Finding site Bone structure false Inferred relationship Some 1
    omodysplasi 2 Occurrence Congenital false Inferred relationship Some 2
    omodysplasi 2 Finding site Bone structure false Inferred relationship Some 2
    omodysplasi 2 Associated morphology kongenital dysplasi false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start