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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


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital/genetic syndrome with poikiloderma Is a Secondary telangiectasia (disorder) false Inferred relationship Some
    Congenital/genetic syndrome with poikiloderma Is a Poikiloderma (disorder) false Inferred relationship Some
    Congenital/genetic syndrome with poikiloderma Associated morphology Telangiectasis false Inferred relationship Some 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Degeneration false Inferred relationship Some
    Congenital/genetic syndrome with poikiloderma Finding site Microscopic skin vascular structure (body structure) false Inferred relationship Some 1
    Congenital/genetic syndrome with poikiloderma Is a Congenital disease false Inferred relationship Some
    Congenital/genetic syndrome with poikiloderma Occurrence Congenital false Inferred relationship Some 3
    Congenital/genetic syndrome with poikiloderma Finding site Skin structure false Inferred relationship Some 2
    Congenital/genetic syndrome with poikiloderma Associated morphology Poikiloderma false Inferred relationship Some 2
    Congenital/genetic syndrome with poikiloderma Finding site Microscopic skin vascular structure (body structure) false Inferred relationship Some 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Telangiectasis false Inferred relationship Some 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Poikiloderma false Inferred relationship Some 2
    Congenital/genetic syndrome with 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 Congenital/genetic syndrome with poikiloderma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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