has material basis in germline mutation in disease has major feature AP1S2 congenital nervous system disorder syndromic X-linked intellectual disability 5 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/pettigrew_syndrome intellectual disability, X-linked, syndromic, fried type MRX59 Pettigrew syndrome SCTID:719139003 mental retardation, X-linked, syndromic, fried type X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome intellectual disability X-linked with Dandy-Walker malformation basal ganglia disease and seizures X-linked intellectual disability 59 Orphanet:85329 mental retardation X-linked syndromic 5 OMIM:304340 Pettigrew syndrome, X-linked recessive X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behaviour syndrome X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (XDIBS), or Pettigrew syndrome is a central nervous system malformation characterized by severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead), and brain imaging abnormalities such as Dandy-Walker malformation, and iron deposition. mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures DOID:0060800 intellectual disability, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures intellectual disability X-linked syndromic 5 PETTIGREW syndrome intellectual disability, X-linked 59 intellectual disability, X-linked syndromic 5 NCIT:C124839 MRXS5 MONDO:0010574 Orphanet:1568 Editor note: check relationship to friend syndrome syndromic X-linked intellectual disability fried type PGS intellectual disability, X-linked, syndromic 5 intellectual disability, X-linked, syndromic 21 Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures mental retardation, X-linked, syndromic 21 syndromic X-linked intellectual disability type 5 MEDGEN:162924 X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - seizures MRXS21 X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome GARD:0008520 UMLS:C0796254 mental retardation, X-linked 59 mental retardation, X-linked, syndromic 5 mental retardation X-linked with Dandy-Walker malformation basal ganglia disease and seizures syndromic X-linked intellectual disability 21 fried syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability central nervous system malformation X-linked syndromic intellectual disability