Global Variome shared LOVD

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Phenotype #0000321153 Individual ID 00430345 Associated disease Gilbert syndrome Phenotype details see paper; ..., persistent hyperbilirubinemia Diagnosis/Initial Gilbert syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite Gilbert Age/Examination 08y (8 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-01-18 12:47:32 +01:00 (CET) Date last edited N/A

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