Phenotype #0000054290

Individual ID 00074467
Associated disease EIG
Phenotype details Four affected individuals over two generations with idiopathic generalizedepilepsy.
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Bernt Popp
Database submission license No license selected
Created by Bernt Popp
Date created 2016-07-03 13:55:27 +02:00 (CEST)
Date last edited N/A

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