RS770791406 NLRP3
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Associated Conditions
Cryopyrin associated periodic syndrome
Hearing loss
autosomal dominant 34
with or without inflammation
Familial cold autoinflammatory syndrome 1
Chronic infantile neurological
cutaneous and articular syndrome
Familial amyloid nephropathy with urticaria AND deafness
Keratitis fugax hereditaria
Inborn genetic diseases
Cryopyrin associated periodic syndrome
Hearing loss
autosomal dominant 34
with or without inflammation
Familial cold autoinflammatory syndrome 1
Other Variants in NLRP3