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