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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
    61500013 Retinoic acid embryopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    61500013 Retinoic acid embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    61501012 Accutane embryopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    61501012 Accutane embryopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    486568014 Fetal isoretinoin syndrome en Synonym (core metadata concept) Active Only initial character 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 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
    2647065013 Fetal isotretinoin syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2816634016 Foetal isotretinoin syndrome en Synonym (core metadata concept) Active Only initial character 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
    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 Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Causative agent (attribute) Tretinoin (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Causative agent (attribute) Product containing isotretinoin (medicinal product) false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Causative agent (attribute) Environmental agent false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Causative agent (attribute) Isotretinoin (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Causative agent (attribute) Tretinoin (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a trouble causé par un médicament false Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    embryopathie causée par l'acide rétinoïque 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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