RS2103174031 NLRP3
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Associated Conditions
Keratitis fugax hereditaria
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Hearing loss
autosomal dominant 34
with or without inflammation
Chronic infantile neurological
cutaneous and articular syndrome
Cryopyrin associated periodic syndrome
NLRP3-related disorder
Keratitis fugax hereditaria
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Hearing loss
autosomal dominant 34
Other Variants in NLRP3