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18735004: Congenital omphalocele (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
31596019 Congenital omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
31597011 Omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
746271010 Congenital omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535837011 Amniocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
31596019 Congenital omphalocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
31596019 Congenital omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
31597011 Omphalocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
31597011 Omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
746271010 Congenital omphalocele (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
746271010 Congenital omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535837011 Amniocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2535837011 Amniocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
380951000274119 Angeborene Omphalozele de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
440621000274116 Nabelschnurbruch de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3383621001000110 Omphalozele de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4450491000241111 omphalocèle congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4450491000241111 omphalocèle congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
380951000274119 Angeborene Omphalozele de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
440621000274116 Nabelschnurbruch de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3383621001000110 Omphalozele de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital omphalocele Is a Congenital anomaly of abdominal wall false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Finding site Umbilical structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Is a Disorder of umbilicus (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Congenital umbilical defect false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Umbilical hernia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Gastroschisis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Is a Congenital anomaly of intestinal tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Intestinal hernia false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Congenital anomaly of abdominal wall false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital omphalocele Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Congenital omphalocele Finding site cavité abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 5
Congenital omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
Congenital omphalocele Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 6
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital omphalocele Finding site Umbilical structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital omphalocele Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Finding site Structure of abdominopelvic viscus false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Finding site Organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Is a Abdominal organ finding false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele Finding site Intra-abdominopelvic structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital omphalocele Is a Congenital umbilical hernia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Gangrenous omphalocele Is a False Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Omphalocele with obstruction Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
exomphale congénitale Is a False Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Beckwith-Wiedemann syndrome (disorder) Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Unspecified omphalocele Is a False Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Hepatomphalocele Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Omphalocele with gangrene Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Omphalocele - irreducible Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Simple omphalocele Is a False Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Shprintzen Goldberg omphalocele syndrome Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Lethal omphalocele with cleft palate syndrome (disorder) Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Familial omphalocele syndrome with facial dysmorphism (disorder) Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder) Is a True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept)
Repair of omphalocele Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2
Gross operation repair of omphalocele, first stage (procedure) Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2
Gross operation repair of omphalocele, second stage Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2
Repair of omphalocele with prosthesis Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2
Repair of omphalocele with staged closure of prosthesis (procedure) Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2
Repair of large omphalocele with prosthesis (procedure) Has focus True Congenital omphalocele Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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