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CBX1-related neurodevelopmental disorder
MONDO:0700367A neurodevelopmental disorder caused by variation in the CBX1 gene. This disorder is characterised by global motor and language developmental delay, intellectual disability, hypotonia, autism spectrum disorder, and variable dysmorphic features.
0 clinical trials for this condition and its sub-types, 0 tagged with CBX1-related neurodevelopmental disorder itself.
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