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Category

Autoinflammatory syndromes

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Behçet's disease
rare immune-mediated small-vessel systemic vasculitis in humans
familial Mediterranean fever
Human disease
Vogt–Koyanagi–Harada syndrome
multisystem disease
periodic fever syndrome
fevers of unknown etiology recurring over months or years
periodic fever, aphthous stomatitis, pharyngitis and adenitis
PFAPA (Periodic fever - aphthous stomatitis- pharyngitis - adenopathy) syndrome is an auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis
Muckle-Wells syndrome
Human disease
Blau syndrome
autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes
PAPA syndrome
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin
systemic-onset juvenile idiopathic arthritis
Systemic inflammatory disorder, and a subtype of juvenile idiopathic arthritis, associated with fever, rash, and arthritis.
VEXAS syndrome
human disease
cryopyrin-associated periodic syndrome
group of rare autosomal dominant diseases
autosomal dominant familial periodic fever
human disease
Majeed syndrome
Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis
hyper-IgD syndrome
Schnitzler syndrome
Human disease