All diseases

OMIM ID
191900
OMIM term:
MUCKLE-WELLS SYNDROME; MWS
Alternative terms:
URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME
UDA SYNDROME
CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2
(∗) Location:
1q44  
(†) Associated OMIM genes:
NLRP3  
(‡) Associated MGI genes:
Nlrp3  

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