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266455006: Ocular albinism, type II (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    396368012 Ocular albinism, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    396369016 Forsius-Eriksson syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    396370015 Aland island eye disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    396371016 Forsius-Eriksson type ocular albinism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    658953010 Ocular albinism, type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    396368012 Ocular albinism, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    396369016 Forsius-Eriksson syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    396370015 Aland island eye disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    396371016 Forsius-Eriksson type ocular albinism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    658953010 Ocular albinism, type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ocular albinism, type II Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    POSSIBLY EQUIVALENT TO association reference set

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