Phenotypes for disease #01889 (FESD (epilepsy, focal, with speech disorder with/without mental retardation (FESD)), OMIM:245570)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000054268 - - - Familial, autosomal dominant - - - - - NeuroMeGen 00074422
0000333605 Seizure, Neurodevelopmental delay - - Unknown 03y - - - - Andreas Laner 00444352
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