Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3330843016 | Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3330844010 | Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3330845011 | PAGOD syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3330846012 | PAGOD (pulmonary hypoplasia, hypoplasia pulmonary artery, agonadism, omphalocele, dextrocardia) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5402843014 | PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5402844015 | PAGOD syndrome is a severe developmental syndrome characterised by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Is a | Gonadal dysgenesis | true | Inferred relationship | Some | ||
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Finding site | Gonadal structure | true | Inferred relationship | Some | 1 | |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR