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)

Global Variome shared LOVD