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234448003: Congenital von Willebrand's disease type II (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    2840382017 Congenital von Willebrand disease type II en Synonym Active Initial character case insensitive SNOMED CT core
    351272019 Congenital von Willebrand's disease type II en Synonym Active Initial character case insensitive SNOMED CT core
    351273012 vWD - Congenital von Willebrand's disease type II en Synonym Active Case sensitive SNOMED CT core
    622767019 Congenital von Willebrand's disease type II (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 II Has interpretation Abnormal false Inferred relationship Some 2
    Congenital von Willebrand's disease type II Interprets Haemostatic function false Inferred relationship Some 2
    Congenital von Willebrand's disease type II Occurrence Congenital false Inferred relationship Some 1
    Congenital von Willebrand's disease type II Finding site Body system structure false Inferred relationship Some
    Congenital von Willebrand's disease type II Has definitional manifestation Haemostatic system finding false Inferred relationship Some
    Congenital von Willebrand's disease type II Is a Congenital von Willebrand's disease false Inferred relationship Some
    Congenital von Willebrand's disease type II 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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