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17604001: Bilateral right-sidedness sequence (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    29749018 Bilateral right-sidedness sequence en Synonym Active Entire term case insensitive SNOMED CT core module
    29750018 Asplenia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    29751019 Splenic agenesis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    29752014 Ivemark syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    29753016 Congenital absence of spleen syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    29754010 Congenital absence of spleen en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    744928010 Bilateral right-sidedness sequence (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    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
    Bilateral right-sidedness sequence Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Is a Laterality sequence false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Is a Congenital anomaly of spleen false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Is a Congenital absence of spleen false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Is a Disorder of spleen false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Bilateral right-sidedness sequence Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Bilateral right-sidedness sequence Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Is a Asplenia false Inferred relationship Existential restriction modifier
    Bilateral right-sidedness sequence Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
    Bilateral right-sidedness sequence Is a Aplasia of spleen false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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