Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5045309018 | Familial chilblain lupus erythematosus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5045314019 | Familial chilblain lupus erythematosus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5045310011 | A rare monogenic form of cutaneous lupus erythematosus characterised by infantile or childhood onset of cold-induced erythematous papules or plaques predominantly on the fingers, toes, nose, cheeks, and ears. Recurrent ulceration of the lesions may lead to necrotic tissue destruction and mutilation. Patients may experience ischaemia of the affected acral regions. Histological findings include cutaneous perivascular inflammatory infiltrates with deposits of immunoglobulins or complement. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5045311010 | A rare monogenic form of cutaneous lupus erythematosus characterized by infantile or childhood onset of cold-induced erythematous papules or plaques predominantly on the fingers, toes, nose, cheeks, and ears. Recurrent ulceration of the lesions may lead to necrotic tissue destruction and mutilation. Patients may experience ischemia of the affected acral regions. Histological findings include cutaneous perivascular inflammatory infiltrates with deposits of immunoglobulins or complement. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial chilblain lupus erythematosus (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Is a | Chilblain lupus erythematosus | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Due to | Lupus erythematosus | true | Inferred relationship | Some | 2 | |
| Familial chilblain lupus erythematosus (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
| Familial chilblain lupus erythematosus (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
| Familial chilblain lupus erythematosus (disorder) | Is a | Chronic disease of skin | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Is a | Chronic disease of immune function (disorder) | true | Inferred relationship | Some | ||
| Familial chilblain lupus erythematosus (disorder) | Clinical course | Chronic | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR