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234447008: Congenital von Willebrand's disease type I (disorder)

    Status: retired, Primitive. Date: 30-Nov 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2841830016 Congenital von Willebrand disease type I en Synonym Active Initial character case insensitive SNOMED CT core
    351270010 vWD - Congenital von Willebrand's disease type I en Synonym Active Case sensitive SNOMED CT core
    351271014 Congenital von Willebrand's disease type I en Synonym Active Initial character case insensitive SNOMED CT core
    622766011 Congenital von Willebrand's disease type I (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital von Willebrand's disease type I Has interpretation Abnormal false Inferred relationship Some 2
    Congenital von Willebrand's disease type I Interprets Haemostatic function false Inferred relationship Some 2
    Congenital von Willebrand's disease type I Occurrence Congenital false Inferred relationship Some 1
    Congenital von Willebrand's disease type I Finding site Body system structure false Inferred relationship Some
    Congenital von Willebrand's disease type I Has definitional manifestation Haemostatic system finding false Inferred relationship Some
    Congenital von Willebrand's disease type I Is a Congenital von Willebrand's disease false Inferred relationship Some
    Congenital von Willebrand's disease type I Finding site Entire haematological system false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian emergency department reference set

    Concept inactivation indicator reference set

    REPLACED BY association reference set

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