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102450007: staafjesmonochromatisme (aandoening)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    165685019 Rod monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    541192016 Rod monochromatism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6972091000146111 complete achromatopsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6972101000146116 typische achromatopsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    8045421000146113 'rod'-monochromatisme nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    8045461000146118 staafjesmonochromatisme (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    8045471000146112 staafjesmonochromatisme nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    staafjesmonochromatisme (aandoening) Is a Achromatopsia false Inferred relationship Some
    staafjesmonochromatisme (aandoening) Finding site Retinal structure false Inferred relationship Some
    staafjesmonochromatisme (aandoening) Occurrence Congenital false Inferred relationship Some
    staafjesmonochromatisme (aandoening) Interprets Vision observable (observable entity) false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Has interpretation Abnormal false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Interprets Visual function false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Has interpretation Abnormal false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Interprets Visual function false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Occurrence Congenital false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Finding site Retinal structure false Inferred relationship Some 1
    staafjesmonochromatisme (aandoening) Associated morphology Dystrophy false Inferred relationship Some 2
    staafjesmonochromatisme (aandoening) Finding site Retinal structure false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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