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37355009: Royer's syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    62317016 Royer's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    62319018 Prader-Willi syndrome AND diabetes en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    769213011 Royer's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2840034017 Royer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    62317016 Royer's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    62319018 Prader-Willi syndrome AND diabetes en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    769213011 Royer's syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    769213011 Royer's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2840034017 Royer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Royer's syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Existential restriction modifier (core metadata concept)
    Royer's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Royer's syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Royer's syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    Royer's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Royer's syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1

    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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