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275261001: Gastrointestinal tract congenital anomaly (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    411221011 GIT congenital anomaly en Synonym Active Entire term case sensitive SNOMED CT core module
    668110013 Gastrointestinal tract congenital anomaly (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
    Gastrointestinal tract congenital anomaly (disorder) Is a Disorder of gastrointestinal tract false Inferred relationship Existential restriction modifier
    Gastrointestinal tract congenital anomaly (disorder) Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
    Gastrointestinal tract congenital anomaly (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier
    Gastrointestinal tract congenital anomaly (disorder) Finding site Gastrointestinal tract structure false Inferred relationship Existential restriction modifier 1
    Gastrointestinal tract congenital anomaly (disorder) Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Gastrointestinal tract congenital anomaly (disorder) Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
    Gastrointestinal tract congenital anomaly (disorder) Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital volvulus Is a False Gastrointestinal tract congenital anomaly (disorder) Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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