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402769003: Congenital/genetic syndrome with poikiloderma (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
    1770693017 Congenital/genetic syndrome with poikiloderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1781863011 Congenital/genetic syndrome with poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1231091000005112 Kongenit/genetisk syndrom med poikiloderma 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
    Kongenit/genetisk syndrom med poikiloderma Is a Secondary telangiectasia (disorder) false Inferred relationship Some
    Kongenit/genetisk syndrom med poikiloderma Is a Poikiloderma (disorder) false Inferred relationship Some
    Kongenit/genetisk syndrom med poikiloderma Associated morphology Telangiectasis false Inferred relationship Some 1
    Kongenit/genetisk syndrom med poikiloderma Associated morphology Degeneration false Inferred relationship Some
    Kongenit/genetisk syndrom med poikiloderma Finding site Microscopic skin vascular structure false Inferred relationship Some 1
    Kongenit/genetisk syndrom med poikiloderma Is a Congenital disease false Inferred relationship Some
    Kongenit/genetisk syndrom med poikiloderma Occurrence Congenital false Inferred relationship Some 3
    Kongenit/genetisk syndrom med poikiloderma Finding site Skin structure false Inferred relationship Some 2
    Kongenit/genetisk syndrom med poikiloderma Associated morphology Poikiloderma false Inferred relationship Some 2
    Kongenit/genetisk syndrom med poikiloderma Finding site Microscopic skin vascular structure false Inferred relationship Some 1
    Kongenit/genetisk syndrom med poikiloderma Associated morphology Telangiectasis false Inferred relationship Some 1
    Kongenit/genetisk syndrom med poikiloderma Associated morphology Poikiloderma false Inferred relationship Some 2
    Kongenit/genetisk syndrom med poikiloderma Finding site Skin structure false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary sclerosing poikiloderma of Weary (disorder) Is a False Kongenit/genetisk syndrom med poikiloderma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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