Phenotype #0000061004

Individual ID 00072158
Associated disease CMD1I
Phenotype details biventricular dilatation (HP:0001713), sick sinus syndrome (HP:0011704), no skeletal muscle atrophy (HP:0003202), muscle weakness (HP:0001324), heart transplantation; 2 maternal cousins died due to sudden cardiac deaths (SCD)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 36y (36 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset sick sinus syndrome (HP:0011704), Left ventricular hypertrophy (HP:0001712)
Protein -
Owner name Pieter Klap
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-10-11 10:05:53 +02:00 (CEST)
Date last edited 2019-03-16 16:19:05 +01:00 (CET)

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