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771145006: Herpetiform pemphigus (disorder)


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


0 descendants.

Expanded Value Set


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

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