Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3472919015 | Acral dystrophic epidermolysis bullosa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3472920014 | Acral dystrophic epidermolysis bullosa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3472921013 | Acral DEB (dystrophic epidermolysis bullosa) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403847016 | A form of localized dystrophic epidermolysis bullosa characterized by trauma-induced blistering confined primarily to the hands and feet. Healing of blisters is associated with milia formation, atrophic scarring and dystrophic nails. There is no extracutaneous involvement. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403848014 | A form of localised dystrophic epidermolysis bullosa characterised by trauma-induced blistering confined primarily to the hands and feet. Healing of blisters is associated with milia formation, atrophic scarring and dystrophic nails. There is no extracutaneous involvement. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acral dystrophic epidermolysis bullosa (disorder) | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
Acral dystrophic epidermolysis bullosa (disorder) | Is a | Localised dystrophic epidermolysis bullosa | true | Inferred relationship | Some | ||
Acral dystrophic epidermolysis bullosa (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Acral dystrophic epidermolysis bullosa (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Acral dystrophic epidermolysis bullosa (disorder) | Finding site | Connective tissue structure | false | Inferred relationship | Some | ||
Acral dystrophic epidermolysis bullosa (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Acral dystrophic epidermolysis bullosa (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Acral dystrophic epidermolysis bullosa (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Acral dystrophic epidermolysis bullosa (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 5 | |
Acral dystrophic epidermolysis bullosa (disorder) | Associated morphology | Epidermolysis | false | Inferred relationship | Some | 4 | |
Acral dystrophic epidermolysis bullosa (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 5 | |
Acral dystrophic epidermolysis bullosa (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Acral dystrophic epidermolysis bullosa (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Acral dystrophic epidermolysis bullosa (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Acral dystrophic epidermolysis bullosa (disorder) | Associated morphology | Epidermolysis | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)