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56848002: Foville-Wilson syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    94537010 Foville-Wilson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    795405011 Foville-Wilson syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    94537010 Foville-Wilson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    795405011 Foville-Wilson syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    795405011 Foville-Wilson syndrome (disorder) en Fully specified name 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
    Foville-Wilson syndrome Is a Disorder of brain stem (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Foville-Wilson syndrome Is a Neurologic disorder of eye movements (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Foville-Wilson syndrome Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways false Inferred relationship Existential restriction modifier (core metadata concept)
    Foville-Wilson syndrome Finding site Pontine structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Foville-Wilson syndrome Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Foville-Wilson syndrome Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Foville-Wilson syndrome Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
    Foville-Wilson syndrome Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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