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234446004: Congenital von Willebrand's disease (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    351268018 Congenital von Willebrand's disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    351269014 vWD - Congenital von Willebrand's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    622765010 Congenital von Willebrand's disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2839593011 Congenital von Willebrand disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1944751000052112 medfödd von Willebrands sjukdom sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    medfödd von Willebrands sjukdom Is a von Willebrand disorder false Inferred relationship Some
    medfödd von Willebrands sjukdom Finding site Entire hematological system (body structure) false Inferred relationship Some
    medfödd von Willebrands sjukdom Is a Congenital disease (disorder) false Inferred relationship Some
    medfödd von Willebrands sjukdom Occurrence Congenital false Inferred relationship Some 1
    medfödd von Willebrands sjukdom Finding site Body system structure false Inferred relationship Some
    medfödd von Willebrands sjukdom Has definitional manifestation Hemostatic system finding false Inferred relationship Some
    medfödd von Willebrands sjukdom Has interpretation Abnormal false Inferred relationship Some 2
    medfödd von Willebrands sjukdom Interprets Hemostatic function false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group
    medfödd von Willebrands sjukdom, typ 1 Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    medfödd von Willebrands sjukdom, typ 2 Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    medfödd von Willebrands sjukdom, typ 3 Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    von Willebrands sjukdom, typ 2F Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    Hereditary von Willebrand disease type 1A Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    von Willebrands sjukdom, typ 1a Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    von Willebrands sjukdom, typ 1A Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    von Willebrands sjukdom, typ 2A Is a False medfödd von Willebrands sjukdom Inferred relationship Some
    von Willebrands sjukdom, typ 2B Is a False medfödd von Willebrands sjukdom Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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