Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1495355018 | Lipoatrophic diabetes mellitus | en | Synonym | Active | Case insensitive | SNOMED CT core |
1495356017 | Total lipoatrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3029639016 | Berardinelli-Seip congenital lipodystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
3029702014 | Congenital generalised lipodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3029742016 | Congenital generalized lipodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3029802015 | Beradinelli-Seip syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
423109014 | Berardinelli's syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
423110016 | Lawrence-Seip syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
423111017 | Seip's syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
423112012 | Congenital total lipodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
678342011 | Congenital total lipodystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Generalised congenital lipodystrophy with myopathy | Is a | True | Congenital generalised lipodystrophy | Inferred relationship | Some | |
Lipodystrophy, intellectual disability, deafness syndrome | Is a | True | Congenital generalised lipodystrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set