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17604001: Bilateral right-sidedness sequence (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    29749018 Bilateral right-sidedness sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    29750018 Asplenia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    29751019 Splenic agenesis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    29752014 Ivemark syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    29753016 Congenital absence of spleen syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    744928010 Bilateral right-sidedness sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1698681000005115 Ivemarks syndom da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ivemarks syndom Is a Disorder of spleen false Inferred relationship Some
    Ivemarks syndom Is a Congenital anomaly of trunk false Inferred relationship Some
    Ivemarks syndom Is a Congenital anomaly of the hematopoietic system false Inferred relationship Some
    Ivemarks syndom Is a Laterality sequence false Inferred relationship Some
    Ivemarks syndom Finding site Splenic structure false Inferred relationship Some 1
    Ivemarks syndom Occurrence Congenital false Inferred relationship Some
    Ivemarks syndom Associated morphology Congenital absence false Inferred relationship Some 1
    Ivemarks syndom Is a Congenital anomaly of spleen false Inferred relationship Some
    Ivemarks syndom Is a Congenital absence of spleen false Inferred relationship Some
    Ivemarks syndom Finding site Splenic structure false Inferred relationship Some 1
    Ivemarks syndom Associated morphology Congenital absence false Inferred relationship Some 1
    Ivemarks syndom Is a Disorder of spleen false Inferred relationship Some
    Ivemarks syndom Occurrence Congenital false Inferred relationship Some 2
    Ivemarks syndom Associated morphology dysgenese false Inferred relationship Some 2
    Ivemarks syndom Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Ivemarks syndom Occurrence Congenital false Inferred relationship Some 1
    Ivemarks syndom Is a Congenital or functional absence of spleen false Inferred relationship Some
    Ivemarks syndom Associated morphology Aplasia false Inferred relationship Some 1
    Ivemarks syndom Is a Aplasia of spleen (disorder) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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