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414929001: Oculodermal melanocytosis (disorder)

    Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2531935013 Oculodermal melanocytosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    2535499015 Oculodermal melanocytosis en Synonym Active Case insensitive SNOMED CT core
    2538077015 Congenital oculodermal melanocytosis en Synonym Active Case insensitive SNOMED CT core
    2538078013 Nevus fuscocerulophthalmomaxillaris en Synonym Active Case insensitive SNOMED CT core
    2538080019 Naevus fuscocerulophthalmomaxillaris en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Oculodermal melanocytosis Is a Mass of eye structure false Inferred relationship Some
    Oculodermal melanocytosis Is a Melanocytic naevus false Inferred relationship Some
    Oculodermal melanocytosis Is a Disorder of eye region false Inferred relationship Some
    Oculodermal melanocytosis Associated morphology Melanocytic naevus - category false Inferred relationship Some 1
    Oculodermal melanocytosis Finding site Eye region structure false Inferred relationship Some 1
    Oculodermal melanocytosis Is a Mass of head and/or neck false Inferred relationship Some
    Oculodermal melanocytosis Is a Mass of eye structure false Inferred relationship Some
    Oculodermal melanocytosis Finding site Eye region structure false Inferred relationship Some 1
    Oculodermal melanocytosis Associated morphology Melanocytic naevus - category false Inferred relationship Some 1
    Oculodermal melanocytosis Is a Mass of head false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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