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270117002: Platelet type pseudo-von Willebrand disease (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
    404988018 Platelet type pseudo-von Willebrand disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    662992013 Platelet type pseudo-von Willebrand disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    404988018 Platelet type pseudo-von Willebrand disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    662992013 Platelet type pseudo-von Willebrand disease (disorder) en Fully specified name 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
    Platelet type pseudo-von Willebrand disease Is a Hereditary platelet function disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Finding site Platelet (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Has definitional manifestation Platelet finding false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Platelet type pseudo-von Willebrand disease Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
    Platelet type pseudo-von Willebrand disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Platelet type pseudo-von Willebrand disease Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Platelet type pseudo-von Willebrand disease Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Platelet type pseudo-von Willebrand disease Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 3

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    SAME AS association reference set (foundation metadata concept)

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