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
03917 ATFB13 fibrillation, atrial, familial, type 13 (ATFB-13) 615377 AD - - SCN1B - -
04170 BRGDA Brugada syndrome (BRGDA) - - 122 99 SCN1B, SCN2B, SCN3B, SCN4B - -
01020 BRGDA5 Brugada syndrome, type 5 (BRGDA-5, conduction defect, cardiac, nonspecific) 612838 - - - SCN1B - -
06420 EIEE52 Epileptic encephalopathy, early infantile, 52 617350 AR - - SCN1B - -
00354 GEFSP1 epilepsy, generalized, with febrile seizures plus, type 1 (GEFSP-1) 604233 AD 1 1 SCN1B - -
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