User:Colin McTroll/Books/Autoinflammatory Diseases
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MAJOR PERIODIC FEVER SYNDROMES
Familial Mediterranean fever
TNF receptor-1 associated periodic syndrome
Hyperimmunoglobulin D syndrome
Cryopyrin-associated periodic syndromes
PFAPA syndrome
OTHER AUTOINFLAMMATORY DISORDERS
Deficiency of the interleukin-1 receptor antagonist
PAPA syndrome
Blau syndrome
Chronic atypical neutrophilic dermatitis with lipodystrophy and elevated temperature
Deficiency of the interleukin-36 receptor antagonist
Chronic recurrent multifocal osteomyelitis
STING-associated vasculopathy with onset in infancy
Nod-like receptor family, caspase recruitment domain-containing 4 or NLR family CARD domain-containing protein 4 (NLRC4)-activating mutations
Linear ubiquitination chain assembly complex deficiency (LUBAC)
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) or PLAID, also called familial cold autoinflammatory syndrome 3 (FCAS3), (APLAID or PLAID) is a form of familial atypical cold urticaria related to 1-Phosphatidylinositol-4,5-bisphosphate phosphodiesterase gamma-2 (PLCG2)