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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
    29749018 Bilateral right-sidedness sequence en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    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 Only initial character 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 Only initial character 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 Only initial character case insensitive (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 Only initial character 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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Bilateral right-sidedness sequence Is a Disorder of spleen false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Is a Laterality sequence false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Is a Congenital anomaly of spleen false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Is a Congenital absence of spleen false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Is a Disorder of spleen false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bilateral right-sidedness sequence Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Bilateral right-sidedness sequence Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Is a Asplenia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Bilateral right-sidedness sequence Associated morphology Aplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Bilateral right-sidedness sequence Is a Aplasia of spleen (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    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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