All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02633 CINCA;CAPS3 CINCA syndrome (CINCCA, cryopyrin-associted periodic syndrome type 3 (CAPS3)) 607115 AD 0 0 NLRP3 - -
06027 DFNA34 Deafness, autosomal dominant 34, with or without inflammation 617772 AD 0 0 NLRP3 - -
01256 FCAS1 autoinflammatory syndrome, cold, familial, type 1 (FCAS-1) 120100 AD 1 1 NLRP3 - -
05990 KEFH Keratoendothelitis fugax hereditaria 148200 AD 0 0 NLRP3 - -
01594 MWS Muckle-Wells syndrome (MWS) 191900 AD 14 14 NLRP3 - -
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