FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

270117002: Platelet type pseudo-von Willebrand 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
    404988018 Platelet type pseudo-von Willebrand disease en Synonym Active Only initial character case insensitive SNOMED CT core module
    662992013 Platelet type pseudo-von Willebrand disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

    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 false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Finding site Platelet false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Has definitional manifestation Platelet finding false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Finding site Body system structure false Inferred relationship Existential restriction modifier 2
    Platelet type pseudo-von Willebrand disease Is a Congenital disease false Inferred relationship Existential restriction modifier
    Platelet type pseudo-von Willebrand disease Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Platelet type pseudo-von Willebrand disease Has interpretation Abnormal false Inferred relationship Existential restriction modifier 3
    Platelet type pseudo-von Willebrand disease Interprets Hemostatic function false Inferred relationship Existential restriction modifier 3
    Platelet type pseudo-von Willebrand disease Interprets Hemostatic function false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start