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1172589000: Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4634492010 Gershoni Baruch syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4634494011 Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4634495012 Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Is a Congenital omphalocele true Inferred relationship Existential restriction modifier
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Finding site Umbilical structure true Inferred relationship Existential restriction modifier 1
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Associated morphology Hernial opening true Inferred relationship Existential restriction modifier 1
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Finding site Structure of organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier 2
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 2
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 3
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 4
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 4
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Finding site Structure of abdominopelvic cavity and/or content true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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