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 |
| 79462015 | Metachromatic leukodystrophy, late infantile type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 494894011 | Metachromatic leucodystrophy, late infantile type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 785168018 | Metachromatic leukodystrophy, late infantile type (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1230504012 | Late infantile metachromatic leucodystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1788033010 | Greenfield disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Metachromatic leukodystrophy, late infantile type | Is a | Arylsulfatase A deficiency | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, late infantile type | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, late infantile type | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Metachromatic leukodystrophy, late infantile 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