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10386005: Congenital thrombocytopenia (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    18079011 Congenital thrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    18080014 Hereditary thrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    556257010 Congenital thrombocytopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    18079011 Congenital thrombocytopenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    18079011 Congenital thrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    18080014 Hereditary thrombocytopenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    18080014 Hereditary thrombocytopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    556257010 Congenital thrombocytopenia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    556257010 Congenital thrombocytopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    66861000077112 thrombocytopénie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    66861000077112 thrombocytopénie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    thrombocytopénie congénitale Is a Thrombocytopenia false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Finding site Platelet (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Is a Thrombocytopenic disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Has definitional manifestation Platelet count below reference range (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
    thrombocytopénie congénitale Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Wiskott-Aldrich syndrome Is a False thrombocytopénie congénitale Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

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

    POSSIBLY EQUIVALENT TO association reference set

    SAME AS association reference set (foundation metadata concept)

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