Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 296970014 | Schulz's disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 296971013 | Schultz disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 576602018 | Schultz disease (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Schultz disease | est un(e) (attribut) | Leucodystrophy without a known biochemical basis | false | Inferred relationship | Some | ||
| Schultz disease | morphologie associée (attribut) | Myelin sheath alteration | false | Inferred relationship | Some | 1 | |
| Schultz disease | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Schultz disease | morphologie associée (attribut) | Myelin sheath alteration | false | Inferred relationship | Some | 1 | |
| Schultz disease | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Schultz disease | localisation d'une constatation (attribut) | système nerveux | false | Inferred relationship | Some | 1 | |
| Schultz disease | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Schultz disease | localisation d'une constatation (attribut) | système nerveux | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR