Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356653011 | Glycogen storage disease type Ic | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 356654017 | Phosphate transport defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626776012 | Phosphate transport defect (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Phosphate transport defect | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Phosphate transport defect | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Phosphate transport defect | Finding site | Liver structure | false | Inferred relationship | Some | ||
| Phosphate transport defect | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | ||
| Phosphate transport defect | Is a | Glycogen storage 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
FHIR