Phenotype #0000291819

Individual ID 00398737
Associated disease FFEVF1
Phenotype details Generalized-onset seizure, Mild global developmental delay, Interictal EEG abnormality; brother also affected (untested)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 12y (12 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2022-01-10 14:09:43 +01:00 (CET)
Date last edited 2022-01-13 21:26:44 +01:00 (CET)

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