Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3687582015 | Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3687583013 | Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | en | Synonym | Active | Case sensitive | SNOMED CT core |
3687587014 | Toxic epidermolysis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3687603019 | An acute and severe skin disease with clinical and histological features of destruction and detachment of the skin epithelium and mucous membranes. Onset may occur at any age, but the risk increases after 40 years. Three subforms have been described according to the percentage of the body surface area affected: Stevens-Johnson syndrome (less than 10%), Lyell syndrome (greater than 30%) and an intermediate form (10-29%). The initial manifestations are nonspecific: a seemingly banal rash, fever, and a burning sensation involving the eyes, mouth and genitalia. The rash rapidly progresses to become vesicular and bullous on the face and body. High fever is a constant feature. Two thirds of cases are triggered by a drug allergy. In rare cases, the disease is associated with infections or bone marrow transplantation. The remaining 25-30% of cases are classed as idiopathic. The prognosis for patients with extensive forms is poor. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Acute eruption of skin | false | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Erythroderma | false | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Clinical course | Acute | true | Inferred relationship | Some | 4 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Skin necrosis | true | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Acute skin disorder | false | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Acute erythematous rash of skin | true | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Is a | Erythematous condition | false | Inferred relationship | Some | ||
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Associated morphology | Necrosis | true | Inferred relationship | Some | 2 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Associated morphology | Erythema | true | Inferred relationship | Some | 1 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Associated morphology | Separation | true | Inferred relationship | Some | 3 | |
Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Finding site | Structure of skin and/or mucous membrane | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Lyell syndrome | Is a | True | Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Inferred relationship | Some | |
Stevens Johnson syndrome AND toxic epidermal necrolysis overlap | Is a | True | Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Inferred relationship | Some | |
Stevens-Johnson syndrome | Is a | True | Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set