Phenotypes for disease #01263 (BFNS2 (seizures, neonatal, benign, familial, type 2 (BFNS-2)), OMIM:121201)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000087538 see paper; … - - Familial, autosomal dominant - - - - - Gaetan Lesca 00111696
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