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36871005: Retinoic acid embryopathy (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
    61500013 Retinoic acid embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    486569018 Fetal vitamin A syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    486570017 Congenital malformation due to vitamin A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    768673017 Retinoic acid embryopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2816635015 Foetal vitamin A syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    68341000077117 embryopathie causée par l'acide rétinoïque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    embryopathie causée par l'acide rétinoïque Is a Multiple malformation syndrome due to non-infectious environmental agents false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Occurrence Congenital false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Causative agent Product containing tretinoin (medicinal product) false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Causative agent Product containing isotretinoin (medicinal product) false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Causative agent Environmental agent false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Causative agent Isotretinoin (substance) false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Causative agent Tretinoin (substance) false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Associated morphology Congenital malformation false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Some
    embryopathie causée par l'acide rétinoïque Occurrence Congenital false Inferred relationship Some 1
    embryopathie causée par l'acide rétinoïque Associated morphology anomalie du développement 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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