Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3663022016 | Familial multiple lipomatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3663023014 | Familial multiple lipomatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3663027010 | A rare benign genetic skin disease with characteristics of numerous, painless, encapsulated lipomas located in the subcutaneous adipose tissue of the trunk and extremities, with relative sparing of the neck and shoulders. Association with gastroduodenal lipomatosis, brain anomalies or lipomatosis, and refractory epilepsy has been reported. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial multiple lipomatosis | Finding site | Subcutaneous tissue structure | true | Inferred relationship | Some | 1 | |
Familial multiple lipomatosis | Is a | Lipomatosis of subcutaneous tissue | true | Inferred relationship | Some | ||
Familial multiple lipomatosis | Associated morphology | Lipomatosis | true | Inferred relationship | Some | 1 | |
Familial multiple lipomatosis | Is a | Familial disease | 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
Description inactivation indicator reference set