All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00137 CINCA CINCA SYNDROM 607115 AD - - NLRP3 - -
00138 DFNA34 DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION 617772 AD - - NLRP3 - -
00139 FCAS1 FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 120100 AD - - NLRP3 - -
00140 KEFH KERATOENDOTHELIITIS FUGAX HEREDITARIA 148200 AD - - NLRP3 - -
00141 MWS MUCKLE-WELLS SYNDROME 191900 AD - - NLRP3 - -
00057 YAOS YAO SYNDROME 617321 Mu - - INS, NLRP3, NOD2 - -
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