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718221007: Behr syndrome (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
    3310335013 Behr syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
    3310359015 Behr syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    3311570019 Infantile hereditary optic atrophy with neurological abnormality en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Behr syndrome Is a Optic atrophy false Inferred relationship Existential restriction modifier
    Behr syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
    Behr syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
    Behr syndrome Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
    Behr syndrome Associated morphology Atrophy false Inferred relationship Existential restriction modifier 1
    Behr syndrome Occurrence Infancy false Inferred relationship Existential restriction modifier 1
    Behr syndrome Finding site Optic nerve 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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