CAMK2D-related neurodevelopmental disorder and dilated cardiomyopathy

MONDO:1040008

A neurodevelopmental disorder caused by variation in the CAMK2D gene. This disorder is characterised by intellectual disability, speech and motor delay, behavioural problems and dilated cardiomyopathy. Patients often present brain structural anomalies and hypotonia, and less frequently, seizures.

24 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by