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

0 clinical trials for this condition and its sub-types, 0 tagged with ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder itself.

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↑ Congenital nervous system disorder (287) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Autosomal dominant syndromic intellectual disability (15)

Including sub-types (0) Tagged with ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder (0)

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