Phenotype #0000000916

Individual ID 00001762
Associated disease SBCADD
Inheritance Familial
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Onset 00y00m03d
Phenotype/Onset -
Phenotype details clinical presentation; developmental delay, epilepsy
Protein -
Age/Diagnosis -
Owner name Division of Human Genetics, Innsbruck
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Division of Human Genetics, Innsbruck
Date created 2013-04-05 13:06:01 +02:00 (CEST)
Date last edited 2013-05-13 09:25:51 +02:00 (CEST)

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