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204746004: Hirschsprung's disease and allied congenital conditions NOS (disorder)

    Status: retired, Primitive. Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    313967014 Hirschsprung's disease and allied congenital conditions NOS en Synonym Active Case sensitive SNOMED CT core
    590013018 Hirschsprung's disease and allied congenital conditions NOS (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 NOS Finding site Colon structure false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions NOS Occurrence Congenital false Inferred relationship Some
    Hirschsprung's disease and allied congenital conditions NOS Finding site Structure of large intestine false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions NOS Associated morphology Congenital anomaly false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions NOS Occurrence Congenital false Inferred relationship Some
    Hirschsprung's disease and allied congenital conditions NOS Finding site Colon structure false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions NOS Associated morphology Congenital anomaly false Inferred relationship Some 1
    Hirschsprung's disease and allied congenital conditions NOS Is a Hirschsprung's disease and allied congenital conditions false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    WAS A association reference set

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