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402769003: Congenital/genetic syndrome with poikiloderma (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770693017 Congenital/genetic syndrome with poikiloderma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    1781863011 Congenital/genetic syndrome with poikiloderma en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital/genetic syndrome with poikiloderma Is a Secondary telangiectasia false Inferred relationship Existential restriction modifier
    Congenital/genetic syndrome with poikiloderma Is a Poikiloderma false Inferred relationship Existential restriction modifier
    Congenital/genetic syndrome with poikiloderma Associated morphology Telangiectasis false Inferred relationship Existential restriction modifier 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Degeneration false Inferred relationship Existential restriction modifier
    Congenital/genetic syndrome with poikiloderma Finding site Microscopic skin vascular structure false Inferred relationship Existential restriction modifier 1
    Congenital/genetic syndrome with poikiloderma Is a Congenital disease false Inferred relationship Existential restriction modifier
    Congenital/genetic syndrome with poikiloderma Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Congenital/genetic syndrome with poikiloderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Congenital/genetic syndrome with poikiloderma Associated morphology Poikiloderma false Inferred relationship Existential restriction modifier 2
    Congenital/genetic syndrome with poikiloderma Finding site Microscopic skin vascular structure false Inferred relationship Existential restriction modifier 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Telangiectasis false Inferred relationship Existential restriction modifier 1
    Congenital/genetic syndrome with poikiloderma Associated morphology Poikiloderma false Inferred relationship Existential restriction modifier 2
    Congenital/genetic syndrome with poikiloderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary sclerosing poikiloderma of Weary Is a False Congenital/genetic syndrome with poikiloderma Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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