Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| 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