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24704003: Cone monochromatism (disorder)


    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
    41406010 Cone monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    754371017 Cone monochromatism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1223986010 Blue cone monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    41406010 Cone monochromatism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    41406010 Cone monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    754371017 Cone monochromatism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    754371017 Cone monochromatism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1223986010 Blue cone monochromatism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1223986010 Blue cone monochromatism en Synonym (core metadata concept) 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
    Cone monochromatism Is a Achromatopsia false Inferred relationship Existential restriction modifier (core metadata concept)
    Cone monochromatism Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Cone monochromatism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Cone monochromatism Interprets Vision observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cone monochromatism Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cone monochromatism Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    REPLACED BY association reference set (foundation metadata concept)

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