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724638006: Splenomegaly co-occurrent and due to storage disease (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
    3442240019 Splenomegaly co-occurrent and due to storage disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3442241015 Splenomegaly co-occurrent and due to storage disease en Synonym Active Entire term case insensitive SNOMED CT core module
    3442242010 Splenomegaly with storage disease en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Splenomegaly co-occurrent and due to storage disease Due to Storage disease false Inferred relationship Existential restriction modifier 2
    Splenomegaly co-occurrent and due to storage disease Is a Splenomegaly false Inferred relationship Existential restriction modifier
    Splenomegaly co-occurrent and due to storage disease Is a Storage disease false Inferred relationship Existential restriction modifier
    Splenomegaly co-occurrent and due to storage disease Is a Hereditary disorder by system false Inferred relationship Existential restriction modifier
    Splenomegaly co-occurrent and due to storage disease Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Splenomegaly co-occurrent and due to storage disease Associated morphology Enlargement false Inferred relationship Existential restriction modifier 3
    Splenomegaly co-occurrent and due to storage disease Finding site Entire spleen false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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