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38209007: Encephalo-ophthalmic dysplasia (disorder)

    Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    63949019 Encephalo-ophthalmic dysplasia en Synonym Active Case insensitive SNOMED CT core
    63950019 Krausse's syndrome en Synonym Active Case sensitive SNOMED CT core
    772056011 Encephalo-ophthalmic dysplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Encephalo-ophthalmic dysplasia Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Pathological process Pathological developmental process false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Occurrence Congenital false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Is a Congenital anomaly of brain false Inferred relationship Some
    Encephalo-ophthalmic dysplasia Associated morphology Congenital anomaly false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Finding site Brain structure false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Occurrence Congenital false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Associated morphology Developmental abnormality false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Finding site Brain structure false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Occurrence Congenital false Inferred relationship Some
    Encephalo-ophthalmic dysplasia Finding site Brain structure false Inferred relationship Some 1
    Encephalo-ophthalmic dysplasia Associated morphology Dysplasia false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Finding site Structure of central nervous system false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Associated morphology Developmental abnormality false Inferred relationship Some 2
    Encephalo-ophthalmic dysplasia Associated morphology Congenital anomaly false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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