Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1234349019 | Oculocerebrorenal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
1234350019 | Cerebro-oculorenal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
1234352010 | Lowe disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
1234353017 | Phosphatidylinositol-4,5-bisphosphate-5-phosphatase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
131703019 | Lowe syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
131704013 | Oculocerebrorenal syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
131705014 | Renal-oculocerebrodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
131706010 | Lowe-Terrey-MacLachlan syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
131707018 | Lowe-Bickel syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3789845014 | Oculocerebrorenal syndrome of Lowe | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
820429012 | Lowe syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Glaucoma due to Lowe syndrome | Due to | True | Lowe syndrome | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set