FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

402769003: Congenital/genetic syndrome with poikiloderma (disorder)

    Status: retired, Primitive. 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 Case insensitive SNOMED CT core
    1781863011 Congenital/genetic syndrome with poikiloderma en Synonym Active Case insensitive 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 false Inferred relationship Some
    Congenital/genetic syndrome with poikiloderma Is a Poikiloderma 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 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 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 Is a False Congenital/genetic syndrome with poikiloderma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

    Back to Start