Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 296972018 | Metachromatic leukodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 296973011 | Sulphatide lipidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 296974017 | Sulfatide lipidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 296975016 | Greenfield disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 296976015 | Metachromatic leucodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 296977012 | MLD | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 296978019 | Familial progressive cerebral sclerosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 296979010 | van Bogaert-Nijssen disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 296980013 | MLD - Metachromatic leucodystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 296981012 | Metachromatic leukoencephaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 576603011 | Metachromatic leucodystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Metachromatic leukodystrophy | Is a | Sphingolipidosis | false | Inferred relationship | Some | ||
| Metachromatic leukodystrophy | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Metachromatic leukodystrophy | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator | Is a | False | Metachromatic leukodystrophy | Inferred relationship | Some | |
| Metachromatic leucodystrophy, congenital type | Is a | False | Metachromatic leukodystrophy | Inferred relationship | Some | |
| Sphingolipid activator protein 1 deficiency | Is a | False | Metachromatic leukodystrophy | Inferred relationship | Some | |
| Metachromatic leukodystrophy without arylsulfatase deficiency | Is a | False | Metachromatic leukodystrophy | Inferred relationship | Some | |
| Arylsulfatase A deficiency | Is a | False | Metachromatic leukodystrophy | Inferred relationship | Some |
Reference Sets
Australian dialect reference set
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set
FHIR