Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3317352014 | 6q terminal deletion syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3317353016 | 6q terminal deletion syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3317354010 | Syndrome marked by a characteristic facial dysmorphism, short neck and psychomotor retardation, generally associated with a range of non-specific malformations. Isolated terminal 6q deletion syndrome is very rare with less than 20 cases being reported in the literature. The most frequent craniofacial anomalies include microcephaly, broad nose with prominent nasal root and bulbous nasal tip, large ears that may be malformed and low-set and a characteristic downturned mouth. The most commonly described neurological features are psychomotor retardation, hypotonia and seizures. Retinal anomalies are also common. The breakpoints are located between chromosome regions 6q25.3 and 6q26, within the fragile site FRA6E. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
6q terminal deletion syndrome | Is a | Anomaly of chromosome pair 6 | false | Inferred relationship | Some | ||
6q terminal deletion syndrome | Is a | Deletion of part of autosome | false | Inferred relationship | Some | ||
6q terminal deletion syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
6q terminal deletion syndrome | Finding site | Chromosome pair 6 | true | Inferred relationship | Some | 2 | |
6q terminal deletion syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
6q terminal deletion syndrome | Finding site | Chromosome pair 6 | true | Inferred relationship | Some | 3 | |
6q terminal deletion syndrome | Associated morphology | Deletion of long arm | true | Inferred relationship | Some | 2 | |
6q terminal deletion syndrome | Associated morphology | Partial monosomy | true | Inferred relationship | Some | 3 | |
6q terminal deletion syndrome | Is a | Deletion of part of long arm of chromosome 6 | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set