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204662000: Other specified esophageal anomalies (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    313824019 Other specified esophageal anomalies en Synonym Active Entire term case insensitive SNOMED CT core module
    313825018 Other specified oesophageal anomalies en Synonym Active Entire term case insensitive SNOMED CT core module
    589918017 Other specified esophageal anomalies (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Other specified esophageal anomalies Is a Congenital anomaly of esophagus false Inferred relationship Existential restriction modifier
    Other specified esophageal anomalies Finding site Esophageal structure false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Occurrence Congenital false Inferred relationship Existential restriction modifier
    Other specified esophageal anomalies Finding site Digestive tract structure false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Occurrence Congenital false Inferred relationship Existential restriction modifier
    Other specified esophageal anomalies Finding site Esophageal structure false Inferred relationship Existential restriction modifier 1
    Other specified esophageal anomalies Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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