Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Hereditary Autoinflammatory Diseases
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Hereditary Autoinflammatory Diseases
Description
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES. MeSH
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Subtype Terms (4)
Behcet Syndrome
38 drugs (32 approved, 6 experimental)
Cryopyrin-Associated Periodic Syndromes
8 drugs (3 approved, 5 experimental)
Familial Mediterranean Fever
8 drugs (6 approved, 2 experimental)
Mevalonate Kinase Deficiency
1 approved drug
Phase 3 Indicated Drugs (3)
Phase 2 Indicated Drugs (1)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (2)
Organization Involved with Phase 2 Indications (6)
Organization Involved with Phase 1 Indications (1)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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