Houge-Janssens syndrome 1

An autosomal dominant intellectual developmental disorder that has material basis in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1.

Also known as: MRD35, autosomal dominant intellectual disability 35, intellectual disability, autosomal dominant type 35, intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome, mental retardation, autosomal dominant type 35, autosomal dominant non-syndromic intellectual disability 35, intellectual disability, autosomal dominant 35, mental retardation, autosomal dominant 35

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