Global Variome shared LOVD

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Phenotype #0000179410 Individual ID 00239192 Associated disease CMH Phenotype details see paper; ... Diagnosis/Initial hypertrophic cardiomyopathy Inheritance Familial, autosomal dominant Diagnosis/Definite CMH-17 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 2019-06-06 15:14:24 +02:00 (CEST) Date last edited N/A

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