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 |
6455451000146117 | syndroom van Joubert met congenitale leverfibrose | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6957281000146115 | cerebellaire-vermis-agenesiesyndroom met congenitale leverfibrose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6957291000146118 | joubertsyndroom met congenitale leverfibrose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6957301000146119 | cerebellaire-vermis-agenesiesyndroom met congenitale leverfibrose (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3326249014 | A very rare subtype of Joubert syndrome with the neurological features of Joubert Syndrome and congenital hepatic fibrosis. Prevalence is unknown. The age of onset and severity of hepatic manifestations are variable. Some patients may also present chorioretinal or optic nerve colobomas and nephronophthisis but these are not mandatory features. Over 70% of cases are due to mutations in the TMEM67 gene (8q22.1). | 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 |
This concept is not in any reference sets