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205924007: [X]Congenital malformation of intestine, unspecified (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    315733013 [X]Congenital malformation of intestine, unspecified en Synonym Active Only initial character case insensitive SNOMED CT core module
    591357016 [X]Congenital malformation of intestine, unspecified (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    [X]Congenital malformation of intestine, unspecified Is a Congenital anomaly of lower alimentary tract false Inferred relationship Existential restriction modifier
    [X]Congenital malformation of intestine, unspecified Occurrence Congenital false Inferred relationship Existential restriction modifier
    [X]Congenital malformation of intestine, unspecified Finding site Intestinal structure false Inferred relationship Existential restriction modifier 1
    [X]Congenital malformation of intestine, unspecified Finding site Lower gastrointestinal tract structure false Inferred relationship Existential restriction modifier 1
    [X]Congenital malformation of intestine, unspecified Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    [X]Congenital malformation of intestine, unspecified Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
    [X]Congenital malformation of intestine, unspecified Occurrence Congenital false Inferred relationship Existential restriction modifier
    [X]Congenital malformation of intestine, unspecified Is a Congenital anomaly of intestinal tract false Inferred relationship Existential restriction modifier
    [X]Congenital malformation of intestine, unspecified Is a Congenital anomaly of lower alimentary tract false Inferred relationship Existential restriction modifier
    [X]Congenital malformation of intestine, unspecified Finding site Lower gastrointestinal tract structure false Inferred relationship Existential restriction modifier 1
    [X]Congenital malformation of intestine, unspecified 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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