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ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder

MONDO:0014379

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ADNP on chromosome 20q13.13.

Also known as: ADNP Syndrome, ADNP syndrome, ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder, HVDAS, Helsmoortel-Van der Aa syndrome, autosomal dominant intellectual disability 28, intellectual disability, autosomal dominant 28, mental retardation, autosomal dominant 28

32 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) Syndromic disease (24) Human disease (14) Developmental defect during embryogenesis (7) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2)
Trials to join now! 14 Not yet recruiting 5 Not yet finished but already full! 3 Completed 10
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