Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3723216017 | Autosomal systemic lupus erythematosus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3723217014 | Autosomal systemic lupus erythematosus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3723218016 | Autosomal SLE (systemic lupus erythematosus) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3723219012 | Familial systemic lupus erythematosus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3723220018 | A rare genetic multisystemic chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, hematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, amongst others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3723221019 | A rare genetic multisystemic chronic autoimmune disease characterised by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, haematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, amongst others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4220711000052113 | autosomal systemisk lupus erythematosus | 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 |
| Autosomal systemic lupus erythematosus (disorder) | Is a | Connective tissue hereditary disorder (disorder) | true | Inferred relationship | Some | ||
| Autosomal systemic lupus erythematosus (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
| Autosomal systemic lupus erythematosus (disorder) | Is a | Systemic lupus erythematosus | true | Inferred relationship | Some | ||
| Autosomal systemic lupus erythematosus (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
| Autosomal systemic lupus erythematosus (disorder) | Finding site | Connective tissue structure | true | Inferred relationship | Some | 1 | |
| Autosomal systemic lupus erythematosus (disorder) | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal systemic lupus erythematosus (disorder) | Is a | Autoimmune connective tissue disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR