Disease #00428

Official abbreviation CMD-1I
Name cardiomyopathy, dilated, type 1I (CMD-1I)
OMIM ID 604765
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DES
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Individuals

1 entry on 1 page. Showing entry 1.
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00072158 26724190-PatIII2 PubMed: Brodehl 2015, Journal: Brodehl 2015 4-generation family, 3 affected (3M) M no Germany Caucasian >48y 0 - - CMD-1I 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) DES DES 1 3 Pieter Klap
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