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95498007: Congenital myelin deficiency of the optic disc (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    158180014 Congenital myelin deficiency of the optic disc en Synonym Active Entire term case insensitive SNOMED CT core module
    839663015 Congenital myelin deficiency of the optic disc (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital myelin deficiency of the optic disc Is a Congenital anomaly of optic disc false Inferred relationship Existential restriction modifier
    Congenital myelin deficiency of the optic disc Finding site Optic disc structure false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital myelin deficiency of the optic disc Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 2
    Congenital myelin deficiency of the optic disc Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Congenital myelin deficiency of the optic disc Finding site Optic disc structure false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Finding site Optic disc structure false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Congenital myelin deficiency of the optic disc Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Congenital myelin deficiency of the optic disc Finding site Optic disc structure false Inferred relationship Existential restriction modifier 2
    Congenital myelin deficiency of the optic disc Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Congenital myelin deficiency of the optic disc Associated morphology Morphologically abnormal structure 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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