has material basis in germline mutation in TRIP12 autosomal dominant non-syndromic intellectual disability Clark-Baraitser syndrome https://rarediseases.info.nih.gov/diseases/9994/clark-baraitser-syndrome https://www.malacards.org/card/clark_baraitser_syndrome MRD49 UMLS:C2931130 GARD:0009994 MESH:C536208 intellectual disability, autosomal dominant 49 autosomal dominant mental retardation 49 DOID:0080234 OMIM:617752 intellectual disability, tall stature, obesity, macrocephaly and typical facial features Orphanet:600731 Clark-Baraitser syndrome MONDO:0030914 OMIM:300602 mental retardation, tall stature, obesity, macrocephaly and typical facial features mental retardation, autosomal dominant 49 MEDGEN:443983