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 |
3308127014 | Joubert syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308128016 | Joubert syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308129012 | Congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. Cognitive abilities are variable, ranging from severe intellectual deficit to normal intelligence. Careful examination of the face shows a characteristic appearance: large head, prominent forehead, high rounded eyebrow. The syndrome is genetically heterogeneous. Seven genes, AHI1 (6q23), NPHP1 (2q13), CEP290 (12q21), TMEM67 (8q22), RPGRIP1L (16q12), ARL13B (3p12.3-q12.3) and CC2D2A (4p15), and two loci on chromosomes 9q34 (JBTS1) and 11p12-q13 (CORS2/JBTS2) have been associated with the disease so far. Transmission is autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Joubert syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Joubert syndrome (disorder) | Is a | Familial aplasia of the vermis | true | Inferred relationship | Some | ||
Joubert syndrome (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Joubert syndrome (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Joubert syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Joubert syndrome (disorder) | Finding site | Cerebellar vermis structure | true | Inferred relationship | Some | 1 | |
Joubert syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Joubert syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Joubert syndrome with ocular defect (disorder) | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some | |
Joubert syndrome with renal defect (disorder) | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some | |
Joubert syndrome with oculorenal defect (disorder) | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some | |
Joubert syndrome with orofaciodigital defect (disorder) | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some | |
Joubert syndrome with Jeune asphyxiating thoracic dystrophy | Is a | True | Joubert syndrome (disorder) | Inferred relationship | Some |
This concept is not in any reference sets