FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

37355009: Royer's syndrome (disorder)

    Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2840034017 Royer syndrome en Synonym Active Case sensitive SNOMED CT core
    62317016 Royer's syndrome en Synonym Active Case sensitive SNOMED CT core
    62318014 Prader-Willi syndrome and diabetes en Synonym Inactive Initial character case insensitive SNOMED CT core
    62319018 Prader-Willi syndrome AND diabetes en Synonym Active Case sensitive SNOMED CT core
    769213011 Royer's syndrome (disorder) en Fully specified name Active Case sensitive 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 Some
    Royer's syndrome Associated morphology Congenital malformation false Inferred relationship Some
    Royer's syndrome Occurrence Congenital false Inferred relationship Some 1
    Royer's syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
    Royer's syndrome Occurrence Congenital false Inferred relationship Some
    Royer's syndrome Finding site Brain structure false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

    Back to Start