Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2915125015 | Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2915128018 | Arylsulfatase deficiency without metachromatic leukodystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5245570018 | Arylsulfatase deficiency without MLD (metachromatic leukodystrophy) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5245571019 | Arylsulphatase deficiency without MLD (metachromatic leukodystrophy) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5245720018 | Arylsulphatase deficiency without metachromatic leucodystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) | Is a | Disorder of lysosomal enzyme | true | Inferred relationship | Some | ||
| Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR