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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
8948871000172115 omphalocèle congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
8989411000172113 défaut congénital de fermeture de la paroi abdominale dans la région ombilicale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7377951000172119 exomphalos nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7377961000172117 congenitale navelbreuk nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7377971000172114 omfalokèle nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7377981000172112 omphalocele nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7377991000172110 omfalocele nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


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 Some
Congenital omphalocele Associated morphology Congenital failure of fusion false Inferred relationship Some 2
Congenital omphalocele Associated morphology Congenital protrusion false Inferred relationship Some 1
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital false Inferred relationship Some
Congenital omphalocele Finding site Umbilical structure true Inferred relationship Some 2
Congenital omphalocele Is a Disorder of umbilicus (disorder) false Inferred relationship Some
Congenital omphalocele Is a Congenital malformation false Inferred relationship Some
Congenital omphalocele Is a Congenital umbilical defect false Inferred relationship Some
Congenital omphalocele Is a Umbilical hernia (disorder) true Inferred relationship Some
Congenital omphalocele Is a Gastroschisis false Inferred relationship Some
Congenital omphalocele Finding site Intestinal structure false Inferred relationship Some 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 1
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Some 1
Congenital omphalocele Is a Congenital anomaly of intestinal tract false Inferred relationship Some
Congenital omphalocele Is a Intestinal hernia false Inferred relationship Some
Congenital omphalocele Is a Congenital anomaly of abdominal wall false Inferred relationship Some
Congenital omphalocele Is a Congenital malformation false Inferred relationship Some
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 4
Congenital omphalocele Associated morphology Congenital anomaly false Inferred relationship Some 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 3
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) true Inferred relationship Some 2
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 3
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Some 5
Congenital omphalocele Finding site cavité abdominale false Inferred relationship Some 5
Congenital omphalocele Occurrence Congenital false Inferred relationship Some 6
Congenital omphalocele Associated morphology Developmental anomaly false Inferred relationship Some 6
Congenital omphalocele Finding site paroi abdominale false Inferred relationship Some 6
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 4
Congenital omphalocele Finding site Umbilical structure false Inferred relationship Some 4
Congenital omphalocele Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 1
Congenital omphalocele Finding site Structure of abdominopelvic viscus false Inferred relationship Some 1
Congenital omphalocele Finding site Structure of organ within abdominopelvic cavity (body structure) false Inferred relationship Some 1
Congenital omphalocele Is a Abdominal organ finding false Inferred relationship Some
Congenital omphalocele Finding site Intra-abdominopelvic structure true Inferred relationship Some 1
Congenital omphalocele Is a Congenital umbilical hernia (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Gangrenous omphalocele Is a False Congenital omphalocele Inferred relationship Some
Omphalocele with obstruction Is a True Congenital omphalocele Inferred relationship Some
exomphale congénitale Is a False Congenital omphalocele Inferred relationship Some
Beckwith-Wiedemann syndrome Is a True Congenital omphalocele Inferred relationship Some
Unspecified omphalocele Is a False Congenital omphalocele Inferred relationship Some
Hepatomphalocele Is a True Congenital omphalocele Inferred relationship Some
Omphalocele with gangrene Is a True Congenital omphalocele Inferred relationship Some
Omphalocele - irreducible Is a True Congenital omphalocele Inferred relationship Some
Simple omphalocele Is a False Congenital omphalocele Inferred relationship Some
Shprintzen Goldberg omphalocele syndrome (disorder) Is a True Congenital omphalocele Inferred relationship Some
Lethal omphalocele with cleft palate syndrome (disorder) Is a True Congenital omphalocele Inferred relationship Some
Familial omphalocele syndrome with facial dysmorphism (disorder) Is a True Congenital omphalocele Inferred relationship Some
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Is a True Congenital omphalocele Inferred relationship Some

Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

Description inactivation indicator reference set

GB English

US English

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