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234447008: Congenital von Willebrand's disease type I (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
    351270010 vWD - Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    351271014 Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    622766011 Congenital von Willebrand's disease type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2841830016 Congenital von Willebrand disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    351270010 vWD - Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    351271014 Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    622766011 Congenital von Willebrand's disease type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2841830016 Congenital von Willebrand disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital von Willebrand's disease type I Is a maladie de von Willebrand congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital von Willebrand's disease type I Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital von Willebrand's disease type I Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital von Willebrand's disease type I Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital von Willebrand's disease type I Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital von Willebrand's disease type I Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital von Willebrand's disease type I Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

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