All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01263 BFNS2 seizures, neonatal, benign, familial, type 2 (BFNS-2) 121201 AD 1 1 KCNQ3 - -
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