Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 493866013 | Metachromatic leucodystrophy, juvenile type | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 493867016 | Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 493868014 | Juvenile metachromatic leucodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 493869018 | Scholz cerebral sclerosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 73989014 | Metachromatic leukodystrophy, juvenile type | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 781478019 | Metachromatic leukodystrophy, juvenile type (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Metachromatic leucodystrophy, juvenile type | Is a | Arylsulfatase A deficiency | false | Inferred relationship | Some | ||
| Metachromatic leucodystrophy, juvenile type | Is a | Metachromatic leukodystrophy | true | Inferred relationship | Some | ||
| Metachromatic leucodystrophy, juvenile type | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Metachromatic leucodystrophy, juvenile type | Occurrence | Congenital | false | 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