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 |
3326243010 | Joubert syndrome with congenital hepatic fibrosis (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326244016 | Joubert syndrome with hepatic defect | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326245015 | Joubert syndrome with congenital hepatic fibrosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326246019 | Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326247011 | COACH syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326248018 | Gentile syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326250014 | COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402712010 | Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402713017 | Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with congenital hepatic fibrosis (CHF). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Is a | Congenital hepatic fibrosis | true | Inferred relationship | Some | ||
Joubert syndrome with congenital hepatic fibrosis (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Joubert syndrome with congenital hepatic fibrosis (disorder) | Is a | Joubert syndrome (disorder) | true | Inferred relationship | Some | ||
Joubert syndrome with congenital hepatic fibrosis (disorder) | Associated morphology | Aplasia | false | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Finding site | Cerebellar vermis structure | false | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Associated morphology | Fibrosis | false | Inferred relationship | Some | 3 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Finding site | Liver structure | false | Inferred relationship | Some | 3 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Associated morphology | Fibrosis | true | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Finding site | Liver structure | true | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Finding site | Cerebellar vermis structure | true | Inferred relationship | Some | 1 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Is a | Congenital anomaly of liver | false | Inferred relationship | Some | ||
Joubert syndrome with congenital hepatic fibrosis (disorder) | Occurrence | Congenital | 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)