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204180005: Other congenital retinal changes (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    313094010 Other congenital retinal changes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    589371013 Other congenital retinal changes (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    313094010 Other congenital retinal changes en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    313094010 Other congenital retinal changes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    589371013 Other congenital retinal changes (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    589371013 Other congenital retinal changes (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Other congenital retinal changes Is a Congenital anomaly of retina false Inferred relationship Existential restriction modifier (core metadata concept)
    Other congenital retinal changes Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Other congenital retinal changes Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Other congenital retinal changes Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Other congenital retinal changes Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Other congenital retinal changes Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Other congenital retinal changes Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Other congenital retinal changes NOS Is a False Other congenital retinal changes Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

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

    WAS A association reference set (foundation metadata concept)

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