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720854004: Cerebroretinal vasculopathy (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    3322297012 Cerebroretinal vasculopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3322298019 Cerebroretinal vasculopathy en Synonym Active Entire term case insensitive SNOMED CT core module
    3322299010 Grand Kaine Fulling syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

    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 Existential restriction modifier
    Cerebroretinal vasculopathy Is a Retinal vascular disorder false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Is a Cerebrovascular disease false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Is a Leukodystrophy false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Finding site Cerebrovascular system structure false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Finding site Structure of blood vessel of retina false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
    Cerebroretinal vasculopathy Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier 3
    Cerebroretinal vasculopathy Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 3
    Cerebroretinal vasculopathy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 2
    Cerebroretinal vasculopathy Finding site Myelinated nerve fiber structure false Inferred relationship Existential restriction modifier 1
    Cerebroretinal vasculopathy Finding site White matter structure of brain and spinal cord false Inferred relationship Existential restriction modifier 2
    Cerebroretinal vasculopathy Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
    Cerebroretinal vasculopathy Associated morphology Myelin sheath alteration 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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