Neurodevelopmental Disorder with Language Impairment, Autism, and Attention Deficit-Hyperactivity Disorder

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant condition caused by mutation(s) in the CAPRIN1 gene, encoding caprin-1. It is characterized by speech and motor delays, language difficulties, behavioral abnormalities, variably impaired intellectual development, mild ocular and distal skeletal anomalies, and nonspecific dysmorphic features.

**Synonyms:** - NEDLAAD