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90036004: Vitelliform dystrophy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    149249010 Vitelliform dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    833056010 Vitelliform dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1235526010 Vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Vitelliform dystrophy Is a Hereditary macular dystrophy false Inferred relationship Some
    Vitelliform dystrophy Is a Autosomal dominant hereditary disorder (disorder) false Inferred relationship Some
    Vitelliform dystrophy Finding site Macula lutea structure false Inferred relationship Some
    Vitelliform dystrophy Associated morphology Dystrophy false Inferred relationship Some 1
    Vitelliform dystrophy Finding site Retinal structure false Inferred relationship Some 1
    Vitelliform dystrophy Finding site Macula lutea structure false Inferred relationship Some 1
    Vitelliform dystrophy Due to Macular vitelliform deposits false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    A rare, genetic, macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region. Is a False Vitelliform dystrophy Inferred relationship Some
    Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region. Is a False Vitelliform dystrophy Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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