Global Variome shared LOVD

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Phenotype #0000258078 Individual ID 00362708 Associated disease MLYCDD Phenotype details see paper; ..., developmental delay, seizures, acidosis, hypoglycaemia, cardiomyopathy Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - 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 2021-04-22 19:49:50 +02:00 (CEST) Date last edited 2021-04-23 15:13:08 +02:00 (CEST)

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