Phenotypes for disease #00428 (CMD-1I (cardiomyopathy, dilated, type 1I (CMD-1I)), OMIM:604765)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000061004 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) - - Familial, autosomal dominant 36y - - sick sinus syndrome (HP:0011704), Left ventricular hypertrophy (HP:0001712) - Pieter Klap 00072158
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