GenTIGSA Gene Database on Rare Genetic Disorders
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Familial Amyloid Nephropathy With Urticaria And Deafness  
Disease Aliases (21)

Amyloid nephropathy with deafness and urticaria

Caps2

Cryopyrin-associated periodic syndrome 2

Familial amyloid nephropathy with urticaria and deafness

Muckle-wells syndrome

Muckle-wells syndrome; mws

Mws

Muckle wells syndrome

Muckle-wells type amyloidosis

Neutrophilic urticaria

Syndrome, muckle-wells

Syndrome, uda

Syndrome, urticaria-deafness-amyloidosis

Syndromes, uda

Syndromes, urticaria-deafness-amyloidosis

Uda syndrome

Uda syndromes

Urticaria-deafness-amyloidosis syndrome

Urticaria deafness amyloidosis syndrome

Urticaria, deafness and amyloidosis

Urticaria-deafness-amyloidosis syndromes

Associated Genes (1)
 

NCBI-RefSeq:  NLRP3   (NLR family pyrin domain containing 3)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Familial amyloid nephropathy with urticaria and deafness OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations