Phenotypes for disease #02502 (FFEVF1 (epilepsy, familial focal, with variable foci, type 1), OMIM:604364)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000288629 Frontal lobe epilepsy since the age of 16 months, right fronto-basal gyration disorder 16mo - Unknown - - - - - Andreas Laner 00395430
0000291819 Generalized-onset seizure, Mild global developmental delay, Interictal EEG abnormality; brother also affected (untested) - - Familial, autosomal dominant 12y - - - - Andreas Laner 00398737
0000351942 Nocturnal seizures, Bilateral tonic-clonic seizure with generalized onset - - Familial, autosomal dominant 12y - - - - Andreas Laner 00466579
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