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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 (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) trouble vasculaire rétinien false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) Cerebrovascular disease false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) Leukodystrophy false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) Cardiovascular system hereditary disorder false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) Hereditary disorder of the visual system false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) localisation d'une constatation (attribut) structure du système vasculaire cérébral false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) localisation d'une constatation (attribut) Structure of blood vessel of retina false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 3
    Cerebroretinal vasculopathy (disorder) morphologie associée (attribut) Myelin sheath alteration false Inferred relationship Some 3
    Cerebroretinal vasculopathy (disorder) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 3
    Cerebroretinal vasculopathy (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 2
    Cerebroretinal vasculopathy (disorder) localisation d'une constatation (attribut) Myelinated nerve fiber structure false Inferred relationship Some 1
    Cerebroretinal vasculopathy (disorder) localisation d'une constatation (attribut) White matter structure of brain and spinal cord (body structure) false Inferred relationship Some 2
    Cerebroretinal vasculopathy (disorder) est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
    Cerebroretinal vasculopathy (disorder) morphologie associée (attribut) 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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