Hyperimmunoglobulinemia D with periodic fever

Hyperimmunoglobinemia D with periodic fever (HIDS) is a rare autoinflammatory disease characterized by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhea, arthralgias and skin signs).

Also known as: HIDS, hyper-IgD syndrome, hyperimmunoglobinemia D with recurrent fever, hyperimmunoglobulinemia D syndrome, partial mevalonate kinase deficiency, hyper IgD syndrome, hyperimmunoglobulinemia D and periodic fever syndrome, periodic fever Dutch type

12 clinical trials for this condition and its sub-types, 2 tagged with Hyperimmunoglobulinemia D with periodic fever itself.