Australia and New Zealand Forum For AutoInflammatory Diseases
Anzfaid, Behcet's disease, Blau Syndrome, Cryopyrin-Associated Periodic Syndromes (CAPS) The mild phenotype is called Familial Cold Autoinflammatory Syndrome (FCAS), the moderate phenotype is known as Muckle–Wells syndrome (MWS), and the severe phenotype is referred to as Neonatal-Onset Multisystem Inflammatory Disease (NOMID)/Chronic Infantile Neurologic Cutaneous Articular Syndrome (CINCA). CANDLE Syndrome, CRIA (Cleavage-resistant RIPK1-Induced Autoinflammatory), Chronic Recurrent multifocal osteomyelitis (CRMO), Deficiency of interleukin one receptor antagonist - DIRA, Deficiency of Adenosine Deaminase 2 (DADA2), Familial Mediterranean Fever (FMF), HA20 (A20 haploinsufficiency), Mevalonate Kinase Deficiency (MKD) also known as HIDS (Hyper-IgD-Syndrome), Hidradenitis Suppurativa (HS), Idiopathic Recurrent Pericarditis, Majeed syndrome, PAPA syndrome (pyogenic Arthritis, Pyoderma gangrenosum and Acne), PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis), SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis), Sarcoidosis, Schnitzler syndrome, Stills Disease, Sweet’s syndrome, TNF receptor-associated periodic fever syndrome (TRAPS), VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic), Yao syndrome (formerly called NOD2-associated autoinflammatory disease.
More information can be found at https://anzfaid.org
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