RS180177501 NLRP3
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Associated Conditions
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Autoinflammatory syndrome
Inborn genetic diseases
Keratitis fugax hereditaria
Hearing loss
autosomal dominant 34
with or without inflammation
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
Other Variants in NLRP3