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79417003: Autosomal dominant oculocutaneous albinism (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    131767016 Autosomal dominant oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    820465019 Autosomal dominant oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1453161000005118 Autosomal dominant okulokutan albinisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal dominant okulokutan albinisme Is a Oculocutaneous albinism false Inferred relationship Some
    Autosomal dominant okulokutan albinisme Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    Autosomal dominant okulokutan albinisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Finding site Skin structure false Inferred relationship Some 3
    Autosomal dominant okulokutan albinisme Associated morphology kongenit mangel false Inferred relationship Some
    Autosomal dominant okulokutan albinisme Occurrence Congenital false Inferred relationship Some
    Autosomal dominant okulokutan albinisme Finding site Structure of skin region false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Finding site Eye structure false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Finding site Eye structure false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Occurrence Congenital false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Occurrence Congenital false Inferred relationship Some 3
    Autosomal dominant okulokutan albinisme Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
    Autosomal dominant okulokutan albinisme Occurrence Congenital false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Autosomal dominant okulokutan albinisme Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Hypopigmentation false Inferred relationship Some 1
    Autosomal dominant okulokutan albinisme Associated morphology Hypopigmentation false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    US English

    REPLACED BY association reference set (foundation metadata concept)

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