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204681008: Unspecified anomalies of esophagus (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    313857017 Unspecified anomalies of oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    313858010 Unspecified anomalies of esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    589941013 Unspecified anomalies of esophagus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1695811000005115 uspecificerede oesophagusanomalier da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    uspecificerede oesophagusanomalier Is a Congenital anomaly of esophagus false Inferred relationship Some
    uspecificerede oesophagusanomalier Finding site Oesophageal structure false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Occurrence Congenital false Inferred relationship Some
    uspecificerede oesophagusanomalier Finding site Digestive organ structure false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Associated morphology dysgenese false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Finding site Entire digestive tract including mouth, esophagus, stomach and intestines. false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Associated morphology kongenit anomali false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Occurrence Congenital false Inferred relationship Some
    uspecificerede oesophagusanomalier Associated morphology kongenit anomali false Inferred relationship Some 1
    uspecificerede oesophagusanomalier Finding site Oesophageal structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    WAS A association reference set

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