Global Variome shared LOVD

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Phenotype #0000302329 Individual ID 00410225 Associated disease ACADVLD Phenotype details see paper; ..., newborn screening, asymptomatic Diagnosis/Initial suspected very long chain acyl-CoA dehydrogenase deficiency Inheritance Unknown Diagnosis/Definite - Age/Examination 17m 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 2022-05-20 15:14:42 +02:00 (CEST) Date last edited N/A

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