cardiomyopathy dilated type 1T

cardiomyopathy dilated type 1T

A congenital disorder (OMIM:613740) characterised by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.

Molecular pathology
Defects in TMPO on chromosome 12q22, which encodes thymopoietin, cause cardiomyopathy dilated type 1T.
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