Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3727901010 | Neonatal scleroderma | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3727902015 | Neonatal scleroderma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3727903013 | A very rare secondary neonatal autoimmune disease with characteristics of neonatal-onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Neonatal scleroderma | Is a | Systemic sclerosis | true | Inferred relationship | Some | ||
| Neonatal scleroderma | Pathological process | Autoimmune process | true | Inferred relationship | Some | 1 | |
| Neonatal scleroderma | Associated morphology | Fibrosis | true | Inferred relationship | Some | 1 | |
| Neonatal scleroderma | Occurrence | Neonatal | true | Inferred relationship | Some | 1 | |
| Neonatal scleroderma | Is a | Neonatal disorder | true | Inferred relationship | Some | ||
| Neonatal scleroderma | Finding site | Connective tissue structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR