Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
786422019 | 17q partial trisomy syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
81340012 | 17q partial trisomy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
17q23.1-q23.2 duplication syndrome | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
Proximal duplication of long arm of chromosome 17 | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
PMP22-RAI1 contiguous gene duplication syndrome | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
17q21.31 microduplication syndrome | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
17q11.2 microduplication syndrome | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
17q12 microduplication syndrome | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some | |
Distal trisomy 17q | Is a | True | 17q partial trisomy syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set