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268208007: Hirschsprung's disease and allied congenital conditions (disorder)

    Status: retired, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2840289012 Hirschsprung disease and allied congenital conditions en Synonym Active Case sensitive SNOMED CT core
    400834018 Hirschsprung's disease and allied congenital conditions en Synonym Active Case sensitive SNOMED CT core
    660921016 Hirschsprung's disease and allied congenital conditions (disorder) en Fully specified name Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hirschsprung's disease and allied congenital conditions Occurrence Congenital false Inferred relationship Some
    Hirschsprung's disease and allied congenital conditions Finding site Colon structure false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions Finding site Structure of large intestine false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions Associated morphology Congenital anomaly false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions Occurrence Congenital false Inferred relationship Some
    Hirschsprung's disease and allied congenital conditions Finding site Colon structure false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions Associated morphology Congenital anomaly false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions Is a Congenital functional disorders of the colon false Inferred relationship Some
    Hirschsprung's disease and allied congenital conditions Occurrence Congenital false Inferred relationship Some 2
    Hirschsprung's disease and allied congenital conditions Finding site Colon structure false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hirschsprung's disease and allied congenital conditions NOS Is a False Hirschsprung's disease and allied congenital conditions Inferred relationship Some

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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