Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Syndromic disease · Rheumatic disorder

Autoinflammatory syndrome

A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease.

21 trials tagged with this condition →

Sarcoidosis 61 trials · 84 incl. sub-types Sub-types →
Systemic-onset juvenile idiopathic arthritis 25 trials
Periodic fever syndrome 2 trials · 25 incl. sub-types Sub-types →
Type 1 interferonopathy 4 trials · 21 incl. sub-types Sub-types →
Autoinflammatory syndrome of childhood 0 trials · 19 incl. sub-types Sub-types →
VEXAS syndrome 18 trials
Adult-onset Still disease 12 trials
Pyoderma gangrenosum 10 trials Sub-types →
Idiopathic recurrent pericarditis 8 trials
PFAPA syndrome 6 trials
Chronic recurrent multifocal osteomyelitis 3 trials · 4 incl. sub-types Sub-types →
SAPHO syndrome 3 trials
Schnitzler syndrome 1 trial
Cherubism 1 trial Sub-types →
CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome 0 trials
F12-associated cold autoinflammatory syndrome 0 trials
PAPASH syndrome 0 trials
Pelger-Huet-like anomaly and episodic fever with abdominal pain 0 trials
SAMD9L-associated autoinflammatory syndrome 0 trials
Sharpin-related autoinflammatory syndrome 0 trials
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation 0 trials
Autoinflammatory disease, X-linked 0 trials
Autoinflammatory disease, multisystem, with immune dysregulation, X-linked 0 trials Sub-types →
Autoinflammatory disease, systemic, with vasculitis 0 trials
Autoinflammatory syndrome with immunodeficiency 0 trials
Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis 0 trials
Autoinflammatory syndrome, familial, Behcet-like 0 trials Sub-types →
Autoinflammatory syndrome due to TBK1 deficiency 0 trials
Early-onset pulmonary and cutaneous vasculitis 0 trials
Granulomatous autoinflammatory syndrome of childhood 0 trials
Infantile onset panniculitis with uveitis and systemic granulomatosis 0 trials
Magic syndrome 0 trials
Neonatal inflammatory skin and bowel disease 0 trials Sub-types →
Neonatal-onset severe multisystemic autoinflammatory disease with increased IL18 0 trials
Psoriasis 14, pustular 0 trials
Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome 0 trials
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome 0 trials