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204681008: Unspecified anomalies of esophagus (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    313857017 Unspecified anomalies of oesophagus en Synonym Active Case insensitive SNOMED CT core
    313858010 Unspecified anomalies of esophagus en Synonym Active Case insensitive SNOMED CT core
    589941013 Unspecified anomalies of esophagus (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Unspecified anomalies of oesophagus Finding site Oesophageal structure false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Occurrence Congenital false Inferred relationship Some
    Unspecified anomalies of oesophagus Finding site Digestive organ structure false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Associated morphology Developmental abnormality false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Finding site Digestive tract structure false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Associated morphology Congenital anomaly false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Occurrence Congenital false Inferred relationship Some
    Unspecified anomalies of oesophagus Associated morphology Congenital anomaly false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Finding site Oesophageal structure false Inferred relationship Some 1
    Unspecified anomalies of oesophagus Is a Congenital anomaly of esophagus 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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