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21972006: hereditaire vitamine D-afhankelijkheid type I (aandoening)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    36865015 Hereditary vitamin D dependency syndrome, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    36866019 ARUDD-I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    36868018 Hereditary selective AND simple deficiency of 1 alpha, 25(OH)>2< D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    751327017 Hereditary vitamin D dependency syndrome, type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    6497731000146118 hereditaire vitamine D-afhankelijkheid type I nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6497741000146114 hereditaire vitamine D-afhankelijkheid type I (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6497751000146112 erfelijke selectieve en enkelvoudige deficiëntie van 1-alfa,25-dihydroxyvitamine D3 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6497841000146115 hereditaire selectieve en enkelvoudige deficiëntie van calcitriol nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    7851931000146111 hereditaire selectieve en enkelvoudige deficiëntie van 1,25(OH)-2-D nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    hereditaire vitamine D-afhankelijkheid type I Is a hereditair syndroom van vitamine D-afhankelijkheid false Inferred relationship Some
    hereditaire vitamine D-afhankelijkheid type I Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
    hereditaire vitamine D-afhankelijkheid type I Finding site Structure of endocrine system (body structure) false Inferred relationship Some
    hereditaire vitamine D-afhankelijkheid type I Occurrence Congenital false Inferred relationship Some 1
    hereditaire vitamine D-afhankelijkheid type I Finding site Structure of endocrine system (body 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 (foundation metadata concept)

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