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Up to: Congenital nervous system disorder · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Autosomal dominant syndromic intellectual disability
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3.
This condition has no sub-types.