Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3727901010 | Neonatal scleroderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3727902015 | Neonatal scleroderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4204411000052116 | neonatal sklerodermi | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Neonatal scleroderma | Is a | Systemic sclerosis | true | Inferred relationship | Some | ||
Neonatal scleroderma | Pathological process (attribute) | 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 |
This concept is not in any reference sets