Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3307378014 | Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3307379018 | Potter sequence cleft lip and palate cardiopathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3307380015 | Thomas syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3307381016 | Thomas syndrome has characteristics of renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5477561000241113 | syndrome de séquence de Potter avec fente labiopalatine et cardiopathie | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Is a | Congenital heart disease | true | Inferred relationship | Some | ||
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 2 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 3 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Finding site | Heart structure | false | Inferred relationship | Some | 3 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Finding site | Heart structure | true | Inferred relationship | Some | 1 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set