Related MeSH Hierarchy (5)
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Vascular » Urticaria » Chronic Urticaria » Chronic Inducible Urticaria » Cryopyrin-Associated Periodic Syndromes
Diseases [C] » Immune System Diseases [C20] » Hypersensitivity » Hypersensitivity, Immediate » Urticaria » Chronic Urticaria » Chronic Inducible Urticaria » Cryopyrin-Associated Periodic Syndromes
Diseases [C] » Pathological Conditions, Signs and Symptoms [C23] » Pathologic Processes » Disease Attributes » Chronic Disease » Chronic Urticaria » Chronic Inducible Urticaria » Cryopyrin-Associated Periodic Syndromes
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Hereditary Autoinflammatory Diseases » Cryopyrin-Associated Periodic Syndromes
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Hereditary Autoinflammatory Diseases » Cryopyrin-Associated Periodic Syndromes
Description
A group of rare autosomal dominant diseases, commonly characterized by atypical URTICARIA (hives) with systemic symptoms that develop into end-organ damage. The atypical hives do not involve T-cell or autoantibody. Cryopyrin-associated periodic syndrome includes three previously distinct disorders: Familial cold autoinflammatory syndrome; Muckle-Wells Syndrome; and CINCA Syndrome, that are now considered to represent a disease continuum, all caused by NLRP3 PROTEIN mutations. MeSH
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Approved Indicated Drugs (2)
Phase 2 Indicated Drugs (6)
Phase 1 Indicated Drugs (1)
Organization Involved with Phase 4 Indications (6)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 2 Indications (5)
Organization Involved with Phase 1 Indications (4)
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UMLS Data
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