Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4168107010 | Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 4168108017 | Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency | Is a | Metachromatic leukodystrophy | true | Inferred relationship | Some | ||
| Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency | Due to | Sphingolipid activator protein 1 deficiency | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR