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 |
3704567019 | A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3704568012 | A rare superficial pemphigus disease characterized by severe intractable pruritus with erythematous or urticarial plaques and vesicles organized in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titers of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3704565010 | Herpetiform pemphigus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3704566011 | Herpetiform pemphigus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Associated morphology | Vesiculobullous rash | false | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Pemphigus | true | Inferred relationship | Some | ||
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Associated morphology | Acantholysis | false | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Finding site | Structure of skin and/or mucous membrane (body structure) | false | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Causative agent | Autoantibody | true | Inferred relationship | Some | 2 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Finding site | Structure of skin and/or skin-associated mucous membrane | false | Inferred relationship | Some | 3 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Pathological process (attribute) | Autoimmune process | false | Inferred relationship | Some | 3 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Associated morphology | A fluid-filled, raised, often translucent lesion, greater than 1 cm in diameter | false | Inferred relationship | Some | 3 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Degenerative skin disorder (disorder) | false | Inferred relationship | Some | ||
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Blister of skin | true | Inferred relationship | Some | ||
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Autoimmune skin disease | true | Inferred relationship | Some | ||
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Chemical-induced dermatological disorder (disorder) | true | Inferred relationship | Some | ||
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Causative agent | Autoantibody | true | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Associated morphology | A fluid-filled, raised, often translucent lesion, greater than 1 cm in diameter | true | Inferred relationship | Some | 1 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Associated morphology | Acantholysis | true | Inferred relationship | Some | 2 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 2 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. | Is a | Acantholysis of skin (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set