RS781561828 NLRP3
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Associated Conditions
Chronic infantile neurological
cutaneous and articular syndrome
Familial amyloid nephropathy with urticaria AND deafness
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Keratitis fugax hereditaria
Hearing loss
autosomal dominant 34
with or without inflammation
Chronic infantile neurological
cutaneous and articular syndrome
Familial amyloid nephropathy with urticaria AND deafness
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Keratitis fugax hereditaria
Other Variants in NLRP3