Global Variome shared LOVD

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Phenotype #0000130186 Individual ID 00165321 Associated disease MC3DN Diagnosis/Initial mitochondrial complex III deficiency Diagnosis/Definite MC3DN-5 Phenotype details see paper; …, neonatal lactic acidosis, hypoglycemia, severe episodes of liver failure Inheritance Familial, autosomal recessive 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 2018-07-09 13:52:22 +02:00 (CEST) Date last edited N/A

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