Global Variome shared LOVD

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Phenotype #0000247276 Individual ID 00329079 Associated disease GSD Phenotype details see paper; ..., hypoglycemia, hepatomegaly Diagnosis/Initial glycogen storage disease Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 10m Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-02-03 15:44:42 +01:00 (CET) Date last edited N/A

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