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CNOT9-related developmental disorder with seizures

MONDO:0700353

A neurodevelopmental disorder caused by variation in the CNOT9 gene. This disorder is characterised by moderate-to-severe intellectual disability, delayed or absent speech development, delayed motor development. Most patients present seizures, muscular hypotonia, facial dysmorphism, and behavioral abnormalities.

0 clinical trials for this condition and its sub-types, 0 tagged with CNOT9-related developmental disorder with seizures itself.

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↑ Mendelian neurodevelopmental disorder (208)

Including sub-types (0) Tagged with CNOT9-related developmental disorder with seizures (0)

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