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

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

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