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Up to: Mendelian neurodevelopmental disorder
DIP2C-related developmental disorder with speech delay
A neurodevelopmental disorder caused by variation in the DIP2C gene. This disorder is characterised by developmental delay primarily affect expressive language and speech articulation. Other variable and non-specific phenotypic features include behavioural abnormalities, variable facial anomalies, hypotonia, and structural cardiac anomalies.
This condition has no sub-types.