Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 73989014 | Metachromatic leukodystrophy, juvenile type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 493866013 | Metachromatic leucodystrophy, juvenile type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 493867016 | Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 493868014 | Juvenile metachromatic leucodystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 493869018 | Scholz cerebral sclerosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 781478019 | Metachromatic leukodystrophy, juvenile type (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Metachromatic leukodystrophy, juvenile type | Is a | Arylsulfatase A deficiency | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, juvenile type | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, juvenile type | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, juvenile type | Is a | Metachromatic leucodystrophy | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR