Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 113595017 | Sphingolipid activator protein 1 deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1233038014 | Saposin B deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 1233039018 | SAPI - Sphingolipid activator protein I deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 808219010 | Sphingolipid activator protein 1 deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Sphingolipid activator protein 1 deficiency | Is a | Metachromatic leukodystrophy | true | Inferred relationship | Some | ||
| Sphingolipid activator protein 1 deficiency | Is a | Metachromatic leukodystrophy | false | Inferred relationship | Some | ||
| Sphingolipid activator protein 1 deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Sphingolipid activator protein 1 deficiency | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency | Due to | True | Sphingolipid activator protein 1 deficiency | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR