FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.3  |  FHIR Version n/a  User: [n/a]

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
    1724991000005118 Retinoinsyreembryopati da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Retinoinsyreembryopati Is a Multiple malformation syndrome due to non-infectious environmental agents false Inferred relationship Some
    Retinoinsyreembryopati Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Some
    Retinoinsyreembryopati Occurrence Congenital false Inferred relationship Some
    Retinoinsyreembryopati Causative agent Product containing tretinoin (medicinal product) false Inferred relationship Some
    Retinoinsyreembryopati Causative agent Product containing isotretinoin (medicinal product) false Inferred relationship Some
    Retinoinsyreembryopati Causative agent Environmental agent false Inferred relationship Some
    Retinoinsyreembryopati Is a lægemiddelrelateret sygdom false Inferred relationship Some
    Retinoinsyreembryopati Causative agent Isotretinoin (substance) false Inferred relationship Some
    Retinoinsyreembryopati Causative agent Tretinoin (substance) false Inferred relationship Some
    Retinoinsyreembryopati Associated morphology Kongenit malformation false Inferred relationship Some
    Retinoinsyreembryopati Is a lægemiddelrelateret sygdom false Inferred relationship Some
    Retinoinsyreembryopati Is a kongenit misdannelsessyndrom som følge af kendt ydre årsag false Inferred relationship Some
    Retinoinsyreembryopati Is a lægemiddelrelateret sygdom false Inferred relationship Some
    Retinoinsyreembryopati Occurrence Congenital false Inferred relationship Some 1
    Retinoinsyreembryopati Associated morphology dysgenese false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start