Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1766089015 | Autosomal dominant epidermolysis bullosa simplex (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1777726013 | Autosomal dominant epidermolysis bullosa simplex | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1786149016 | EBS 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Is a | Epidermolysis bullosa simplex | true | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Associated morphology | Epidermolysis | true | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Connective tissue structure | false | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Associated morphology | Keratolysis | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Associated morphology | Blister | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant epidermolysis bullosa simplex (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Epidermolysis bullosa simplex, Ogna type (disorder) | Is a | True | Autosomal dominant epidermolysis bullosa simplex (disorder) | Inferred relationship | Some | |
Epidermolysis bullosa simplex with circinate migratory erythema (disorder) | Is a | True | Autosomal dominant epidermolysis bullosa simplex (disorder) | Inferred relationship | Some | |
Weber-Cockayne syndrome | Is a | True | Autosomal dominant epidermolysis bullosa simplex (disorder) | Inferred relationship | Some | |
Intermediate epidermolysis bullosa simplex with cardiomyopathy (disorder) | Is a | True | Autosomal dominant epidermolysis bullosa simplex (disorder) | Inferred relationship | Some |
This concept is not in any reference sets