Intellectual disability, autosomal dominant 30

Any intellectual disability-expressive aphasia-facial dysmorphism syndrome in which the cause of the disease is a mutation in the ZMYND11 gene.

Also known as: MRD30, ZMYND11 intellectual disability-expressive aphasia-facial dysmorphism syndrome, autosomal dominant intellectual disability 30, intellectual disability, autosomal dominant 30, intellectual disability, autosomal dominant type 30, intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in ZMYND11, mental retardation, autosomal dominant type 30, autosomal dominant non-syndromic intellectual disability 30

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 30 itself.