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36871005: Retinoic acid embryopathy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    61500013 Retinoic acid embryopathy en Synonym Active Entire term case insensitive SNOMED CT core module
    486569018 Fetal vitamin A syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
    486570017 Congenital malformation due to vitamin A en Synonym Active Only initial character case insensitive SNOMED CT core module
    768673017 Retinoic acid embryopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2816635015 Foetal vitamin A syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Retinoic acid embryopathy Is a Multiple malformation syndrome due to non-infectious environmental agents false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Occurrence Congenital false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Causative agent Product containing tretinoin false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Causative agent Product containing isotretinoin false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Causative agent Environmental agent false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Is a Drug-related disorder false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Causative agent Isotretinoin false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Causative agent Tretinoin false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Is a Drug-related disorder false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Is a Drug-related disorder false Inferred relationship Existential restriction modifier
    Retinoic acid embryopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Retinoic acid embryopathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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