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234446004: Congenital von Willebrand's disease (disorder)

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital von Willebrand's disease Is a von Willebrand disorder false Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease Is a Congenital disease false Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Congenital von Willebrand's disease Finding site Body system structure false Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease Has interpretation Abnormal false Inferred relationship Existential restriction modifier 2
    Congenital von Willebrand's disease Interprets Hemostatic function false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital von Willebrand's disease type I Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease type II Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    Congenital von Willebrand's disease type III Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    von Willebrand disease, type IIF Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    Hereditary von Willebrand disease type 1A Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    von Willebrand disease, type 1^a^ Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    von Willebrand disease type IA Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    von Willebrand disease type 2A Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier
    von Willebrand disease type 2B Is a False Congenital von Willebrand's disease Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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