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716172002: Oculocerebral dysplasia syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    3304963016 Oculocerebral dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3304964010 Oculocerebral dysplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    3304965011 Behrens Baumann Vogel syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    3304966012 Microphthalmia and optic nerve aplasia 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
    Oculocerebral dysplasia syndrome Is a Microphthalmos false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Is a Congenital anomaly of optic nerve false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 2
    Oculocerebral dysplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Oculocerebral dysplasia syndrome Finding site Entire eye false Inferred relationship Existential restriction modifier 2
    Oculocerebral dysplasia syndrome Associated morphology Aplasia false Inferred relationship Existential restriction modifier 3
    Oculocerebral dysplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Oculocerebral dysplasia syndrome Finding site Optic nerve structure false Inferred relationship Existential restriction modifier 3
    Oculocerebral dysplasia syndrome Is a Aplasia of optic nerve false Inferred relationship Existential restriction modifier
    Oculocerebral dysplasia syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Oculocerebral dysplasia syndrome Finding site Optic nerve structure false Inferred relationship Existential restriction modifier 1
    Oculocerebral dysplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Oculocerebral dysplasia syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Oculocerebral dysplasia syndrome Associated morphology Aplasia 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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