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720854004: Cerebroretinal vasculopathy (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3322297012 Cerebroretinal vasculopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3322298019 Cerebroretinal vasculopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3322299010 Grand Kaine Fulling syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3322300019 A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy characterized by strokes, vision loss, migraines, pseudotumors, dementia and occasionally renal disease. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3322301015 A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy characterised by strokes, vision loss, migraines, pseudotumours, dementia and occasionally renal disease. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Cerebroretinal vasculopathy Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    Cerebroretinal vasculopathy Is a Retinal vascular disorder (disorder) false Inferred relationship Some
    Cerebroretinal vasculopathy Is a Cerebrovascular disease false Inferred relationship Some
    Cerebroretinal vasculopathy Is a Leucodystrophy false Inferred relationship Some
    Cerebroretinal vasculopathy Is a Cardiovascular system hereditary disorder false Inferred relationship Some
    Cerebroretinal vasculopathy Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Some
    Cerebroretinal vasculopathy Finding site Cerebrovascular system structure false Inferred relationship Some
    Cerebroretinal vasculopathy Finding site Structure of blood vessel of retina (body structure) false Inferred relationship Some
    Cerebroretinal vasculopathy Associated morphology Dystrophy false Inferred relationship Some 3
    Cerebroretinal vasculopathy Associated morphology Myelin sheath alteration false Inferred relationship Some 3
    Cerebroretinal vasculopathy Finding site Structure of nervous system (body structure) false Inferred relationship Some 3
    Cerebroretinal vasculopathy Associated morphology Dystrophy false Inferred relationship Some 2
    Cerebroretinal vasculopathy Finding site Myelinated nerve fiber structure false Inferred relationship Some 1
    Cerebroretinal vasculopathy Finding site White matter structure of brain and spinal cord (body structure) false Inferred relationship Some 2
    Cerebroretinal vasculopathy Is a Hereditary disorder of nervous system false Inferred relationship Some
    Cerebroretinal vasculopathy Associated morphology Myelin sheath alteration false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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