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Up to: Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties
A neurodevelopmental disorder in which the cause of the disease is a mutation in the DPH5 gene. It is characterized by craniofacial dysmorphology, profound neurodevelopmental delay, multisystem abnormalities, and miscarriages.
This condition has no sub-types.