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WDR5-related neurodevelopmental disorder

MONDO:0700365

A neurodevelopmental disorder caused by variation in the WDR5 gene. This disorder is characterised by speech and language delay, motor development delay and/or intellectual disability. Other phenotypic features commonly reported include hypotonia, epilepsy, and behavioural abnormalities.

0 clinical trials for this condition and its sub-types, 0 tagged with WDR5-related neurodevelopmental disorder itself.

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↑ Mendelian neurodevelopmental disorder (208)

Including sub-types (0) Tagged with WDR5-related neurodevelopmental disorder (0)

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