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 InternationalCreative Commons License
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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