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18735004: Congenital omphalocele (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
31596019 Congenital omphalocele en Synonym Active Entire term case insensitive SNOMED CT core module
31597011 Omphalocele en Synonym Active Entire term case insensitive SNOMED CT core module
746271010 Congenital omphalocele (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2535837011 Amniocele en Synonym Active Entire term case insensitive SNOMED CT core 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
Congenital omphalocele Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier 2
Congenital omphalocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 2
Congenital omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital omphalocele Finding site Umbilical structure true Inferred relationship Existential restriction modifier 2
Congenital omphalocele Is a Disorder of umbilicus false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Congenital malformation false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Congenital umbilical defect false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Umbilical hernia true Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Gastroschisis false Inferred relationship Existential restriction modifier
Congenital omphalocele Finding site Intestinal structure false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 1
Congenital omphalocele Is a Congenital anomaly of intestinal tract false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Intestinal hernia false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Congenital anomaly of abdominal wall false Inferred relationship Existential restriction modifier
Congenital omphalocele Is a Congenital malformation false Inferred relationship Existential restriction modifier
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 3
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 4
Congenital omphalocele Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 4
Congenital omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 3
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 3
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 4
Congenital omphalocele Associated morphology Hernial opening true Inferred relationship Existential restriction modifier 2
Congenital omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 3
Congenital omphalocele Associated morphology Herniated structure false Inferred relationship Existential restriction modifier 5
Congenital omphalocele Finding site Abdominopelvic cavity structure false Inferred relationship Existential restriction modifier 5
Congenital omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Congenital omphalocele Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Congenital omphalocele Finding site Abdominal wall structure false Inferred relationship Existential restriction modifier 6
Congenital omphalocele Associated morphology Hernial opening false Inferred relationship Existential restriction modifier 4
Congenital omphalocele Finding site Umbilical structure false Inferred relationship Existential restriction modifier 4
Congenital omphalocele Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital omphalocele Finding site Structure of abdominopelvic viscus false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Finding site Structure of organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier 1
Congenital omphalocele Is a Abdominal organ finding false Inferred relationship Existential restriction modifier
Congenital omphalocele Finding site Structure of abdominopelvic cavity and/or content true Inferred relationship Existential restriction modifier 1
Congenital omphalocele Is a Congenital umbilical hernia true Inferred relationship Existential restriction modifier

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

This concept is not in any reference sets

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