Global Variome shared LOVD

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Phenotype #0000279222 Individual ID 00385427 Associated disease CHTD Phenotype details see paper; ..., tetralogy of Fallot, pulmonary atresia, myxomatous and prolapsed mitral and tricuspid valves, supraventricular tachycardia Diagnosis/Initial tetralogy of Fallot Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset 19w fetal acho tetralogy of Fallot Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-10-11 11:30:49 +02:00 (CEST) Date last edited 2021-10-11 11:39:43 +02:00 (CEST)

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