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 |
| 68053016 | Metachromatic leukodystrophy, congenital type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 492787017 | Metachromatic leucodystrophy, congenital type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 777513018 | Metachromatic leukodystrophy, congenital 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, congenital type | Is a | Metachromatic leucodystrophy | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, congenital type | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, congenital type | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, congenital type | Is a | Metachromatic leucodystrophy | true | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, congenital type | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, congenital type | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR