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234450006: Congenital von Willebrand's disease type III (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    2839595016 Congenital von Willebrand disease type III en Synonym Active Initial character case insensitive SNOMED CT core
    351276016 Congenital von Willebrand's disease type III en Synonym Active Initial character case insensitive SNOMED CT core
    351277013 vWD - Congenital von Willebrand's disease type III en Synonym Active Case sensitive SNOMED CT core
    622770015 Congenital von Willebrand's disease type III (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 III Has interpretation Abnormal false Inferred relationship Some 2
    Congenital von Willebrand's disease type III Interprets Haemostatic function false Inferred relationship Some 2
    Congenital von Willebrand's disease type III Occurrence Congenital false Inferred relationship Some 1
    Congenital von Willebrand's disease type III Finding site Body system structure false Inferred relationship Some
    Congenital von Willebrand's disease type III Has definitional manifestation Haemostatic system finding false Inferred relationship Some
    Congenital von Willebrand's disease type III Is a Congenital von Willebrand's disease false Inferred relationship Some
    Congenital von Willebrand's disease type III Finding site Entire haematological system false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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