Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3638358012 | Distal trisomy 6q | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3638359016 | Distal trisomy 6q (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3638360014 | Distal duplication 6q | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3638361013 | A rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 6. The disorder has a highly variable phenotype with typical characteristics of growth and developmental delay, intellectual disability, craniofacial dysmorphism (microcephaly, flat facial profile, frontal bossing, hypertelorism, downward-slanting palpebral fissures, flat nasal bridge, anteverted nares, bow shaped mouth, micrognathia), short webbed neck and joint contractures. Cardiac, urogenital, ophthalmologic and hand and foot anomalies, as well as umbilical hernia, spasticity and seizures are other features that have been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Distal trisomy 6q | Is a | 6q partial trisomy syndrome | true | Inferred relationship | Some | ||
Distal trisomy 6q | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 1 | |
Distal trisomy 6q | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Distal trisomy 6q | Finding site | Chromosome pair 6 | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set