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 |
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