Global Variome shared LOVD

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Phenotype #0000342155 Individual ID 00453497 Associated disease MADD Phenotype details see paper; ..., newborn screening Diagnosis/Initial multiple acyl-CoA dehydrogenase deficiency Inheritance Familial, autosomal recessive Diagnosis/Definite MADD Age/Examination - 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 2024-09-07 22:14:40 +02:00 (CEST) Date last edited N/A

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