Global Variome shared LOVD

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Phenotype #0000328674 Individual ID 00438776 Associated disease CMH Phenotype details Hypertrophic cardiomyopathy (HCM) + Patent ductus arteriosus (PDA) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 00y04m (4 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Barbara Vona Database submission license Creative Commons Attribution 4.0 International Created by Barbara Vona Date created 2023-10-24 13:25:40 +02:00 (CEST) Date last edited 2023-10-24 18:54:29 +02:00 (CEST)

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