Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 795306013 | Congenital anomaly of subcutaneous tissue (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 94399014 | Congenital anomaly of subcutaneous tissue | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 94400019 | Congenital anomaly of subcutaneous tissue, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Lipodystrophy, intellectual disability, deafness syndrome | Is a | True | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Mandibuloacral dysostosis | Is a | True | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Progeroid and marfanoid aspect, lipodystrophy syndrome | Is a | True | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Congenital diffuse lipomatosis | Is a | False | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Neurofibromatosis type 1 | Is a | False | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Fordyce's disease | Is a | False | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some | |
| Hereditary oedema of legs | Is a | False | Congenital anomaly of subcutaneous tissue | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set