FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

616981000000101: Unspecified omphalocele (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2012. Module: SNOMED CT United Kingdom clinical extension module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1363131000000117 Unspecified omphalocele (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
    1363141000000114 Unspecified omphalocele en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Unspecified omphalocele Is a Congenital omphalocele false Inferred relationship Existential restriction modifier
    Unspecified omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier
    Unspecified omphalocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier 1
    Unspecified omphalocele Associated morphology Herniated structure false Inferred relationship Existential restriction modifier 1
    Unspecified omphalocele Finding site Intestinal structure false Inferred relationship Existential restriction modifier 1
    Unspecified omphalocele Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier 2
    Unspecified omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 2
    Unspecified omphalocele Finding site Umbilical structure false Inferred relationship Existential restriction modifier 2
    Unspecified omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 3
    Unspecified omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 3
    Unspecified omphalocele Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 4
    Unspecified omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 4

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start