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["Table S3. Collected known candidate genes of NDDs."]
["Gene_symbol_alias","Hugo_symbol","Recurrent_in_10_NDD_publications","PMID:25363760 (ASD)","PMID:26402605 (ASD)","PMID:27479843 (ID)","PMID:28135719 (UDD)","PMID:28191889 (ASD)","PMID:28263302 (ASD)","PMID:29262854 (ASD,ID,DD,SCZ)","PMID:29346770 (ASD)","PMID:30559488 (ASD,ID,DD)","PMID:31981491 (ASD)","SFARI_gene-score","SFARI_syndromic","SFARI_number-of-reports","SFARI_number-autism-reports","OMIM_Phenotypes"]
["ARID1B","ARID1B",10,"Y","Y","Y","Y","Y","Y","Y","Y","Y","Y",1,0,44,27,"-"]
["POGZ","POGZ",10,"Y","Y","Y","Y","Y","Y","Y","Y","Y","Y",1,0,30,18,"-"]
["SCN2A","SCN2A",10,"Y","Y","Y","Y","Y","Y","Y","Y","Y","Y",1,0,62,33,"Epileptic encephalopathy, early infantile, 11, 613721 (3), Autosomal dominant; Seizures, benign familial infantile, 3, 607745 (3), Autosomal dominant"]
["ADNP","ADNP",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,39,23,"-"]
["CHD8","CHD8",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,49,34,"{Autism, susceptibility to, 18}, 615032 (3), Autosomal dominant"]
["DYRK1A","DYRK1A",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,42,20,"Mental retardation, autosomal dominant 7, 614104 (3), Autosomal dominant"]
["GRIN2B","GRIN2B",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,53,21,"Epileptic encephalopathy, early infantile, 27, 616139 (3), Autosomal dominant; Mental retardation, autosomal dominant 6, 613970 (3), Autosomal dominant"]
["KMT5B,SUV420H1","KMT5B",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,11,8,"Mental retardation, autosomal dominant 51, 617788 (3), Autosomal dominant"]
["PTEN","PTEN",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,61,24,"Cowden syndrome 1, 158350 (3), Autosomal dominant; {Glioma susceptibility 2}, 613028 (3); Lhermitte-Duclos syndrome, 158350 (3), Autosomal dominant; Macrocephaly/autism syndrome, 605309 (3), Autosomal dominant; {Meningioma}, 607174 (3), Autosomal dominant; Prostate cancer, somatic, 176807 (3)"]
["SYNGAP1","SYNGAP1",9,"Y","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,54,17,"Mental retardation, autosomal dominant 5, 612621 (3), Autosomal dominant"]
["ANK2","ANK2",8,"Y","Y","-","-","Y","Y","Y","Y","Y","Y",1,0,14,13,"-"]
["ANKRD11","ANKRD11",8,"-","-","Y","Y","Y","Y","Y","Y","Y","Y",1,0,43,14,"-"]
["ASH1L","ASH1L",8,"Y","Y","-","-","Y","Y","Y","Y","Y","Y",1,0,15,10,"Mental retardation, autosomal dominant 52, 617796 (3), Autosomal dominant"]
["ASXL3","ASXL3",8,"-","-","Y","Y","Y","Y","Y","Y","Y","Y",1,0,23,12,"-"]
["CHD2","CHD2",8,"-","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,36,16,"Epileptic encephalopathy, childhood-onset, 615369 (3), Autosomal dominant"]
["FOXP1","FOXP1",8,"-","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,49,22,"Mental retardation with language impairment and with or without autistic features, 613670 (3), Autosomal dominant"]
["MYT1L","MYT1L",8,"-","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,18,8,"Mental retardation, autosomal dominant 39, 616521 (3), Autosomal dominant"]
["SLC6A1","SLC6A1",8,"-","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,24,14,"-"]
["TBR1","TBR1",8,"Y","Y","-","-","Y","Y","Y","Y","Y","Y",1,0,26,10,"Intellectual developmental disorder with autism and speech delay, 606053 (3), Autosomal dominant"]
["WAC","WAC",8,"-","Y","-","Y","Y","Y","Y","Y","Y","Y",1,0,17,6,"-"]
["GABRB3","GABRB3",7,"Y","Y","-","Y","Y","-","-","Y","Y","Y",2,0,37,21,"{Epilepsy, childhood absence, susceptibility to, 5}, 612269 (3); Epileptic encephalopathy, early infantile, 43, 617113 (3), Autosomal dominant"]
["TCF7L2","TCF7L2",7,"-","Y","-","-","Y","Y","Y","Y","Y","Y",2,0,3,2,"-"]
["BCL11A","BCL11A",7,"Y","Y","-","Y","-","-","Y","Y","Y","Y",1,0,16,7,"-"]
["CTNNB1","CTNNB1",7,"-","-","Y","Y","Y","-","Y","Y","Y","Y",1,0,21,6,"Colorectal cancer, somatic, 114500 (3); Exudative vitreoretinopathy 7, 617572 (3), Autosomal dominant; Hepatocellular carcinoma, somatic, 114550 (3); Medulloblastoma, somatic, 155255 (3); Mental retardation, autosomal dominant 19, 615075 (3), Autosomal dominant; Ovarian cancer, somatic, 167000 (3); Pilomatricoma, somatic, 132600 (3)"]
["DSCAM","DSCAM",7,"-","Y","-","-","Y","Y","Y","Y","Y","Y",1,0,8,7,"-"]
["PPP2R5D","PPP2R5D",7,"-","-","Y","Y","Y","-","Y","Y","Y","Y",1,0,14,5,"Mental retardation, autosomal dominant 35, 616355 (3), Autosomal dominant"]
["SPAST","SPAST",7,"-","Y","-","-","Y","Y","Y","Y","Y","Y",1,0,10,8,"-"]
["CACNA2D3","CACNA2D3",6,"Y","-","-","-","Y","Y","Y","Y","-","Y",2,0,6,5,"-"]
["PHF2","PHF2",6,"-","Y","-","-","Y","Y","Y","Y","-","Y",2,0,5,5,"-"]
["TBL1XR1","TBL1XR1",6,"-","-","-","Y","Y","-","Y","Y","Y","Y",2,0,20,6,"Mental retardation, autosomal dominant 41, 616944 (3), Autosomal dominant; Pierpont syndrome, 602342 (3), Autosomal dominant"]
["TNRC6B","TNRC6B",6,"-","Y","-","-","Y","Y","Y","Y","Y","-",2,0,7,6,"-"]
["CUL3","CUL3",6,"Y","Y","-","-","Y","Y","Y","-","Y","-",1,0,21,13,"-"]
["DDX3X","DDX3X",6,"-","-","Y","Y","Y","Y","-","Y","Y","-",1,0,19,5,"Mental retardation, X-linked 102, 300958 (3), X-linked recessive, X-linked dominant"]
["KDM6B","KDM6B",6,"-","Y","-","-","-","Y","Y","Y","Y","Y",1,0,11,7,"-"]
["MED13L","MED13L",6,"-","-","-","Y","Y","-","Y","Y","Y","Y",1,0,32,14,"Mental retardation and distinctive facial features with or without cardiac defects, 616789 (3), Autosomal dominant; Transposition of the great arteries, dextro-looped 1, 608808 (3), Autosomal dominant"]
["NAA15","NAA15",6,"-","Y","-","-","Y","Y","Y","Y","Y","-",1,0,13,7,"Mental retardation, autosomal dominant 50, 617787 (3), Autosomal dominant"]
["SETD5","SETD5",6,"-","Y","-","Y","Y","-","Y","-","Y","Y",1,0,24,6,"Mental retardation, autosomal dominant 23, 615761 (3), Autosomal dominant"]
["TRIP12","TRIP12",6,"-","Y","-","-","Y","-","Y","Y","Y","Y",1,0,16,13,"Mental retardation, autosomal dominant 49, 617752 (3), Autosomal dominant"]
["PPM1D","PPM1D",5,"-","-","Y","Y","Y","-","Y","-","Y","-",3,1,6,3,"Breast cancer, somatic, 114480 (3); Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold, 617450 (3), Autosomal dominant"]
["KDM5B","KDM5B",5,"-","Y","-","Y","-","-","Y","-","Y","Y",2,0,13,8,"-"]
["DNMT3A","DNMT3A",5,"-","Y","-","-","-","Y","Y","-","Y","Y",1,0,14,8,"-"]
["GIGYF1","GIGYF1",5,"-","Y","-","-","-","Y","Y","Y","-","Y",1,0,7,6,"-"]
["KMT2A,MLL","KMT2A",5,"-","-","Y","Y","-","Y","Y","-","Y","-",1,0,20,5,"-"]
["KMT2C,MLL3","KMT2C",5,"Y","Y","-","-","-","Y","-","-","Y","Y",1,0,16,11,"-"]
["SHANK3","SHANK3",5,"-","Y","-","-","-","Y","Y","-","Y","Y",1,0,81,42,"Phelan-McDermid syndrome, 606232 (3), Autosomal dominant; {Schizophrenia 15}, 613950 (3), Autosomal dominant"]
["STXBP1","STXBP1",5,"-","-","-","Y","Y","-","Y","-","Y","Y",1,0,40,11,"Epileptic encephalopathy, early infantile, 4, 612164 (3), Autosomal dominant"]
["TCF20","TCF20",5,"-","-","Y","Y","-","-","Y","-","Y","Y",1,0,10,3,"-"]
["TCF4","TCF4",5,"-","-","-","Y","Y","-","Y","-","Y","Y",1,0,44,8,"-"]
["WDFY3","WDFY3",5,"-","Y","-","-","Y","Y","Y","-","Y","-",1,0,17,13,"-"]
["GATAD2B","GATAD2B",4,"-","-","Y","Y","-","-","Y","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 18, 615074 (3), Autosomal dominant"]
["PURA","PURA",4,"-","-","Y","Y","-","-","Y","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 31, 616158 (3), Autosomal dominant"]
["DIP2A","DIP2A",4,"-","Y","-","-","Y","-","-","Y","-","Y",2,0,6,6,"-"]
["DYNC1H1","DYNC1H1",4,"-","-","-","Y","-","Y","-","-","Y","Y",2,0,14,10,"Charcot-Marie-Tooth disease, axonal, type 20, 614228 (3), Autosomal dominant; Mental retardation, autosomal dominant 13, 614563 (3), Autosomal dominant; Spinal muscular atrophy, lower extremity-predominant 1, AD, 158600 (3), Autosomal dominant"]
["ILF2","ILF2",4,"-","Y","-","-","Y","-","Y","Y","-","-",2,0,4,4,"-"]
["KCNQ3","KCNQ3",4,"-","-","-","Y","-","-","Y","-","Y","Y",2,0,9,5,"-"]
["KMT2E,MLL5","KMT2E",4,"-","Y","-","-","-","-","Y","Y","-","Y",2,1,8,6,"-"]
["PAX5","PAX5",4,"-","-","-","-","Y","Y","Y","-","-","Y",2,0,6,6,"-"]
["AHDC1","AHDC1",4,"-","-","Y","Y","-","-","Y","-","Y","-",1,0,11,2,"-"]
["CNOT3","CNOT3",4,"-","-","-","Y","-","Y","Y","-","Y","-",1,0,7,4,"-"]
["CREBBP","CREBBP",4,"-","-","-","Y","-","-","Y","-","Y","Y",1,0,28,9,"-"]
["EHMT1","EHMT1",4,"-","-","Y","Y","-","-","Y","-","Y","-",1,0,23,7,"-"]
["KATNAL2","KATNAL2",4,"Y","Y","-","-","Y","-","Y","-","-","-",1,0,11,9,"-"]
["DLG4","LLGL1",4,"-","-","Y","-","Y","-","Y","-","Y","-",1,0,11,4,"-"]
["MBD5","MBD5",4,"-","Y","-","-","-","-","Y","-","Y","Y",1,0,33,14,"Mental retardation, autosomal dominant 1, 156200 (3), Autosomal dominant"]
["MECP2","MECP2",4,"-","-","-","Y","Y","Y","-","-","Y","-",1,0,81,24,"{Autism susceptibility, X-linked 3}, 300496 (3), X-linked; Encephalopathy, neonatal severe, 300673 (3), X-linked recessive; Mental retardation, X-linked syndromic, Lubs type, 300260 (3), X-linked recessive; Mental retardation, X-linked, syndromic 13, 300055 (3), X-linked recessive; Rett syndrome, 312750 (3), X-linked dominant; Rett syndrome, atypical, 312750 (3), X-linked dominant; Rett syndrome, preserved speech variant, 312750 (3), X-linked dominant"]
["NCKAP1","NCKAP1",4,"-","Y","-","-","Y","-","Y","Y","-","-",1,0,8,6,"-"]
["NRXN1","NRXN1",4,"-","Y","-","-","Y","-","Y","-","-","Y",1,0,82,40,"Pitt-Hopkins-like syndrome 2, 614325 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 17}, 614332 (3)"]
["NSD1","NSD1",4,"-","-","-","Y","-","-","Y","-","Y","Y",1,0,16,8,"-"]
["SRCAP","SRCAP",4,"-","-","Y","-","Y","-","Y","-","Y","-",1,0,5,4,"-"]
["TLK2","TLK2",4,"-","-","-","-","-","-","Y","Y","Y","Y",1,0,14,5,"Mental retardation, autosomal dominant 57, 618050 (3), Autosomal dominant"]
["TRIO","TRIO",4,"-","Y","-","Y","-","-","-","Y","Y","-",1,0,24,11,"Mental retardation, autosomal dominant 44, 617061 (3), Autosomal dominant"]
["GNAI1","GNAI1",4,"-","-","-","Y","-","-","Y","-","Y","Y","-","-","-","-","-"]
["KAT6B","KAT6B",4,"-","-","Y","Y","-","-","Y","-","Y","-","-","-","-","-","-"]
["EEF1A2","EEF1A2",3,"-","-","-","Y","-","-","Y","-","Y","-","NA",1,8,1,"Epileptic encephalopathy, early infantile, 33, 616409 (3), Autosomal dominant; Mental retardation, autosomal dominant 38, 616393 (3), Autosomal dominant"]
["NFIX","NFIX",3,"-","-","-","Y","-","-","Y","-","Y","-","NA",1,10,0,"-"]
["PRR12","PRR12",3,"-","-","-","-","-","-","Y","-","Y","Y","NA",1,2,0,"-"]
["SMARCA2","SMARCA2",3,"-","-","-","Y","-","-","Y","-","Y","-","NA",1,16,4,"-"]
["COL4A3BP,CERT,GPBP","CERT1",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 34, 616351 (3), Autosomal dominant"]
["CSNK2A1","CSNK2A2",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","Okur-Chung neurodevelopmental syndrome, 617062 (3), Autosomal dominant"]
["GABRB2","GABRB2",3,"-","-","-","-","-","-","Y","-","Y","Y","-","-","-","-","Epileptic encephalopathy, infantile or early childhood, 2, 617829 (3), Autosomal dominant"]
["GNAO1","GNAO1",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","Epileptic encephalopathy, early infantile, 17, 615473 (3), Autosomal dominant; Neurodevelopmental disorder with involuntary movements, 617493 (3), Autosomal dominant"]
["ZBTB18","ZBTB18",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 22, 612337 (3), Autosomal dominant"]
["MEF2C","MEF2C",3,"-","-","-","Y","-","-","Y","-","Y","-",3,1,34,9,"Chromosome 5q14.3 deletion syndrome, 613443 (4), Autosomal dominant; Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations, 613443 (3), Autosomal dominant"]
["SATB2","SATB2",3,"-","-","-","Y","-","-","Y","-","Y","-",3,1,28,8,"-"]
["TRAF7","TRAF7",3,"-","-","-","-","-","-","Y","-","Y","Y",3,1,4,2,"-"]
["AGO1","AGO1",3,"-","-","-","-","-","-","Y","Y","Y","-",2,0,7,3,"-"]
["CACNA1E","CACNA1E",3,"-","-","-","-","-","-","Y","-","Y","Y",2,0,10,4,"Epileptic encephalopathy, early infantile, 69, 618285 (3), Autosomal dominant"]
["FOXP2","FOXP2",3,"-","-","-","-","-","-","Y","-","Y","Y",2,0,42,14,"-"]
["HIVEP3","HIVEP3",3,"-","-","-","-","Y","-","Y","-","Y","-",2,0,6,6,"-"]
["KAT6A","KAT6A",3,"-","-","-","Y","-","-","Y","-","Y","-",2,1,12,3,"Mental retardation, autosomal dominant 32, 616268 (3), Autosomal dominant"]
["KCNQ2","KCNQ2",3,"-","-","-","Y","-","-","Y","-","Y","-",2,0,24,3,"Epileptic encephalopathy, early infantile, 7, 613720 (3), Autosomal dominant; Myokymia, 121200 (3), Autosomal dominant; Seizures, benign neonatal, 1, 121200 (3), Autosomal dominant"]
["PTK7","PTK7",3,"-","Y","-","-","Y","-","-","-","-","Y",2,0,4,3,"-"]
["SET","SET",3,"-","-","-","Y","-","-","Y","-","Y","-",2,0,4,1,"Mental retardation, autosomal dominant 58, 618106 (3), Autosomal dominant"]
["ZC3H4","ZC3H4",3,"-","-","-","-","Y","-","Y","Y","-","-",2,0,3,3,"-"]
["AUTS2,KIAA0442","AUTS2",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,38,18,"Mental retardation, autosomal dominant 26, 615834 (3), Autosomal dominant"]
["CASK","CASK",3,"-","-","-","Y","Y","-","-","-","Y","-",1,0,15,4,"FG syndrome 4, 300422 (3); Mental retardation and microcephaly with pontine and cerebellar hypoplasia, 300749 (3), X-linked dominant; Mental retardation, with or without nystagmus, 300422 (3)"]
["CHAMP1","CHAMP1",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,5,1,"Mental retardation, autosomal dominant 40, 616579 (3), Autosomal dominant"]
["CTCF","CTCF",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,14,4,"Mental retardation, autosomal dominant 21, 615502 (3), Autosomal dominant"]
["EP300","EP300",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,17,4,"-"]
["FOXG1","FOXG1",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,26,4,"-"]
["HNRNPU","HNRNPU",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,14,4,"Epileptic encephalopathy, early infantile, 54, 617391 (3), Autosomal dominant"]
["IQSEC2","IQSEC2",3,"-","-","-","Y","Y","-","-","-","Y","-",1,0,25,4,"Mental retardation, X-linked 1/78, 309530 (3), X-linked dominant"]
["IRF2BPL","IRF2BPL",3,"-","Y","-","-","-","-","-","-","Y","Y",1,0,6,4,"Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures, 618088 (3), Autosomal dominant"]
["KANSL1","KANSL1",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,2,1,"-"]
["PACS1","PACS1",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,6,2,"-"]
["PHIP","PHIP",3,"-","-","-","-","Y","-","Y","-","Y","-",1,0,11,3,"Developmental delay, intellectual disability, obesity, and dysmorphic features, 617991 (3), Autosomal dominant"]
["RELN","RELN",3,"Y","-","-","-","Y","-","-","Y","-","-",1,0,52,28,"-"]
["RAI1","RNASE12",3,"-","-","-","-","-","-","Y","-","Y","Y",1,0,21,7,"-"]
["SCN1A","SCN1A",3,"-","-","-","Y","-","-","-","Y","-","Y",1,0,59,21,"Epilepsy, generalized, with febrile seizures plus, type 2, 604403 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 6 (Dravet syndrome), 607208 (3), Autosomal dominant; Febrile seizures, familial, 3A, 604403 (3), Autosomal dominant; Migraine, familial hemiplegic, 3, 609634 (3), Autosomal dominant"]
["SCN8A","SCN8A",3,"-","-","-","Y","-","-","Y","-","Y","-",1,0,34,6,"?Cognitive impairment with or without cerebellar ataxia, 614306 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 13, 614558 (3), Autosomal dominant; Seizures, benign familial infantile, 5, 617080 (3), Autosomal dominant"]
["SETBP1","SETBP1",3,"-","-","-","-","Y","-","Y","-","Y","-",1,0,13,6,"Mental retardation, autosomal dominant 29, 616078 (3), Autosomal dominant; Schinzel-Giedion midface retraction syndrome, 269150 (3), Autosomal dominant"]
["SETD2","SETD2",3,"-","-","-","-","Y","-","Y","-","Y","-",1,0,12,8,"-"]
["SHANK2","SHANK2",3,"-","Y","-","-","-","Y","-","-","-","Y",1,0,34,19,"{Autism susceptibility 17}, 613436 (3)"]
["SIN3A","SIN3A",3,"-","-","-","-","-","-","Y","-","Y","Y",1,0,8,5,"-"]
["UPF3B","UPF3B",3,"-","-","-","Y","-","Y","-","-","Y","-",1,0,13,3,"-"]
["ASXL1","ASXL1",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","-"]
["CHD4","CHD4",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","-"]
["KCNH1","KCNH1",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","-"]
["PUF60","PUF60",3,"-","-","-","Y","-","-","Y","-","Y","-","-","-","-","-","-"]
["VEZF1","VEZF1",3,"-","-","-","-","-","-","Y","-","Y","Y","-","-","-","-","-"]
["WDR45","WDR45",3,"-","-","-","Y","Y","-","-","-","Y","-","-","-","-","-","-"]
["CACNA1A","CACNA1A",2,"-","-","Y","-","-","-","Y","-","-","-","NA",1,16,5,"Epileptic encephalopathy, early infantile, 42, 617106 (3), Autosomal dominant; Episodic ataxia, type 2, 108500 (3), Autosomal dominant; Migraine, familial hemiplegic, 1, 141500 (3), Autosomal dominant; Migraine, familial hemiplegic, 1, with progressive cerebellar ataxia, 141500 (3), Autosomal dominant; Spinocerebellar ataxia 6, 183086 (3), Autosomal dominant"]
["CDK13","CDK13",2,"-","-","-","Y","-","-","-","-","Y","-","NA",1,9,2,"Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360 (3), Autosomal dominant"]
["HDAC8","HDAC8",2,"-","-","-","Y","-","-","-","-","Y","-","NA",1,6,0,"-"]
["POU3F3","POU3F3",2,"-","-","-","-","-","-","Y","-","Y","-","NA",1,1,0,"-"]
["PRKD1","PRKD1",2,"-","-","-","-","-","-","Y","-","Y","-","NA",1,4,2,"Congenital heart defects and ectodermal dysplasia, 617364 (3), Autosomal dominant"]
["SMC1A","SMC1A",2,"-","-","-","Y","-","-","-","-","Y","-","NA",1,6,1,"-"]
["USP9X","USP9X",2,"-","-","-","Y","-","-","-","-","Y","-","NA",1,7,0,"Mental retardation, X-linked 99, 300919 (3), X-linked recessive; Mental retardation, X-linked 99, syndromic, female-restricted, 300968 (3), X-linked dominant"]
["VAMP2","VAMP2",2,"-","-","-","-","-","-","Y","-","Y","-","NA",1,2,1,"-"]
["WDR26","WDR26",2,"-","-","-","-","-","-","Y","-","Y","-","NA",1,5,3,"-"]
["BRPF1","BRPF1",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","Intellectual developmental disorder with dysmorphic facies and ptosis, 617333 (3), Autosomal dominant"]
["CLTC","CLTC",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 56, 617854 (3), Autosomal dominant"]
["DNM1","DNM1",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","Epileptic encephalopathy, early infantile, 31, 616346 (3), Autosomal dominant"]
["KIF11","KIF11",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, 152950 (3), Autosomal dominant"]
["KIF1A","KIF1A",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 9, 614255 (3), Autosomal dominant; Neuropathy, hereditary sensory, type IIC, 614213 (3), Autosomal recessive; Spastic paraplegia 30, autosomal recessive, 610357 (3), Autosomal recessive"]
["PPP2R1A","PPP2R1A",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","Mental retardation, autosomal dominant 36, 616362 (3), Autosomal dominant"]
["TAB2","TAB2",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","Congenital heart defects, nonsyndromic, 2, 614980 (3), Autosomal dominant"]
["ARID2","ARID2",2,"-","-","-","-","-","-","Y","-","Y","-",3,1,6,2,"-"]
["CAMK2A","CAMK2A",2,"-","-","-","-","-","-","Y","Y","-","-",3,1,8,2,"Mental retardation, autosomal dominant 53, 617798 (3), Autosomal dominant; ?Mental retardation, autosomal recessive 63, 618095 (3), Autosomal recessive"]
["FBXO11","FBXO11",2,"-","-","-","-","-","-","Y","-","Y","-",3,1,5,2,"Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, 618089 (3), Autosomal dominant"]
["SMC3","SMC3",2,"-","-","-","-","Y","-","-","-","Y","-",3,1,9,3,"-"]
["ACHE","ACHE",2,"-","Y","-","-","-","-","-","-","Y","-",2,0,4,4,"-"]
["AGAP2","AGAP2",2,"-","-","-","-","-","Y","-","-","Y","-",2,0,4,4,"-"]
["CAPRIN1","CAPRIN1",2,"-","-","-","-","Y","-","-","-","Y","-",2,0,4,2,"-"]
["CDC42BPB","CDC42BPB",2,"-","-","-","-","Y","-","-","-","Y","-",2,0,7,6,"-"]
["CLASP1","CLASP1",2,"-","-","-","-","-","Y","-","-","Y","-",2,0,3,3,"-"]
["CNKSR2","CNKSR2",2,"-","-","-","Y","-","-","-","-","Y","-",2,1,5,1,"-"]
["CTTNBP2","CTTNBP2",2,"Y","Y","-","-","-","-","-","-","-","-",2,0,8,6,"-"]
["DEAF1","DEAF1",2,"-","-","-","-","-","-","-","-","Y","Y",2,1,17,7,"?Dyskinesia, seizures, and intellectual developmental disorder, 617171 (3), Autosomal recessive; Mental retardation, autosomal dominant 24, 615828 (3), Autosomal dominant"]
["DPYSL2","DPYSL2",2,"-","-","-","-","-","-","-","Y","-","Y",2,0,12,3,"-"]
["GRIA2","GRIA2",2,"-","-","-","-","Y","-","-","-","-","Y",2,0,3,2,"-"]
["HECW2","HECW2",2,"-","-","-","-","-","-","Y","-","Y","-",2,0,7,2,"Neurodevelopmental disorder with hypotonia, seizures, and absent language, 617268 (3), Autosomal dominant"]
["KAT2B","KAT2B",2,"-","Y","-","-","Y","-","-","-","-","-",2,0,6,6,"-"]
["KCNS3","KCNS3",2,"-","-","-","-","-","-","Y","-","Y","-",2,0,4,3,"-"]
["KDM6A","KDM6A",2,"-","-","-","-","-","Y","-","-","Y","-",2,0,7,2,"-"]
["LEO1","LEO1",2,"-","-","-","-","-","-","Y","-","Y","-",2,0,3,2,"-"]
["MFRP","MFRP",2,"-","Y","-","-","Y","-","-","-","-","-",2,0,6,6,"-"]
["QRICH1","QRICH1",2,"-","-","-","-","-","-","Y","-","Y","-",2,0,4,2,"-"]
["RANBP17","RANBP17",2,"-","Y","-","-","-","-","Y","-","-","-",2,0,6,5,"-"]
["SMAD4","SMAD4",2,"-","-","-","Y","-","-","-","-","Y","-",2,0,4,2,"-"]
["SRSF11","SRSF11",2,"-","-","-","-","-","Y","-","-","Y","-",2,0,4,3,"-"]
["UBN2","UBN2",2,"-","-","-","-","Y","Y","-","-","-","-",2,0,4,4,"-"]
["ZMYND11","ZMYND11",2,"-","-","-","-","Y","-","-","-","Y","-",2,0,10,3,"Mental retardation, autosomal dominant 30, 616083 (3), Autosomal dominant"]
["BRAF","BRAF",2,"-","-","-","Y","-","-","-","-","Y","-",1,0,8,1,"-"]
["CDKL5","CDKL5",2,"-","-","-","Y","-","-","-","-","Y","-",1,0,36,11,"Epileptic encephalopathy, early infantile, 2, 300672 (3), X-linked dominant"]
["EBF3","EBF3",2,"-","-","-","-","-","-","Y","-","Y","-",1,0,7,2,"-"]
["HECTD4","HECTD4",2,"-","-","-","-","-","-","Y","-","-","Y",1,0,4,4,"-"]
["HIVEP2","HIVEP2",2,"-","-","-","-","-","-","Y","-","Y","-",1,0,8,0,"Mental retardation, autosomal dominant 43, 616977 (3), Autosomal dominant"]
["MEIS2","MEIS2",2,"-","-","-","-","-","-","Y","-","Y","-",1,0,7,2,"Cleft palate, cardiac defects, and mental retardation, 600987 (3), Autosomal dominant"]
["KIAA2022,NEXMIF","NEXMIF",2,"-","-","-","-","-","Y","-","-","Y","-",1,0,20,6,"Mental retardation, X-linked 98, 300912 (3), X-linked dominant"]
["NLGN3","NLGN3",2,"-","Y","-","-","-","Y","-","-","-","-",1,0,34,20,"{Asperger syndrome susceptibility, X-linked 1}, 300494 (3), Isolated cases, X-linked, Multifactorial; {Autism susceptibility, X-linked 1}, 300425 (3), X-linked"]
["PHF21A","PHF21A",2,"-","-","-","-","-","-","-","-","Y","Y",1,0,8,2,"-"]
["PHF3","PHF3",2,"-","-","-","-","-","Y","-","-","Y","-",1,0,4,4,"-"]
["PTPN11","PTPN11",2,"-","-","-","Y","-","-","-","-","Y","-",1,0,16,5,"-"]
["SMARCC2","SMARCC2",2,"-","-","-","-","-","Y","-","-","-","Y",1,0,11,7,"-"]
["SON","SON",2,"-","-","-","-","-","-","Y","-","Y","-",1,0,4,2,"-"]
["SOX5","SOX5",2,"-","-","Y","-","-","-","-","-","Y","-",1,0,14,4,"-"]
["TAOK1","TAOK1",2,"-","-","-","-","-","-","-","-","Y","Y",1,0,2,1,"-"]
["ZNF292","ZNF292",2,"-","-","-","-","Y","-","-","-","Y","-",1,0,5,4,"-"]
["ANP32A","ANP32A",2,"-","-","-","-","Y","-","-","-","Y","-","-","-","-","-","-"]
["ARHGAP5","ARHGAP5",2,"-","-","-","-","Y","-","-","Y","-","-","-","-","-","-","-"]
["DVL3","DVL3",2,"-","-","-","-","Y","-","-","-","Y","-","-","-","-","-","-"]
["EFTUD2","EFTUD2",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["FAM104A","FAM104A",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["FOSL2","FOSL2",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["HIST1H1E","H1-4",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["HIST1H2AC","H2AC6",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["HDLBP","HDLBP",2,"-","-","-","-","-","-","-","Y","-","Y","-","-","-","-","-"]
["ITPR1","ITPR1",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","-"]
["KCND3","KCND3",2,"-","-","-","-","-","-","-","Y","Y","-","-","-","-","-","-"]
["LAMC3","LAMC3",2,"-","-","-","-","Y","-","Y","-","-","-","-","-","-","-","-"]
["LARP4B","LARP4B",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["MAP2K1","MAP2K1",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["MIB1","MIB1",2,"Y","Y","-","-","-","-","-","-","-","-","-","-","-","-","-"]
["MSL3","MSL3",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","-"]
["MYO1E","MYO1E",2,"-","-","-","-","-","-","-","Y","Y","-","-","-","-","-","-"]
["NAA10","NAA10",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","-"]
["WHSC1","NSD2",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["PDHA1","PDHA1",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","-"]
["PHF12","PHF12",2,"-","-","-","-","-","-","-","-","Y","Y","-","-","-","-","-"]
["RAB11A","RAB11A",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["RPL26","RPL26",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["SLC35A2","SLC35A2",2,"-","-","Y","Y","-","-","-","-","-","-","-","-","-","-","-"]
["SYNCRIP","SYNCRIP",2,"-","-","-","-","Y","-","-","-","Y","-","-","-","-","-","-"]
["TCF12","TCF12",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["TNPO2","TNPO2",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["TNPO3","TNPO3",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["UNC80","UNC80",2,"-","-","-","-","Y","-","-","-","Y","-","-","-","-","-","-"]
["WNT7B","WNT7B",2,"-","-","-","-","Y","-","Y","-","-","-","-","-","-","-","-"]
["ZBTB7A","ZBTB7A",2,"-","-","-","-","-","-","Y","-","Y","-","-","-","-","-","-"]
["ZC4H2","ZC4H2",2,"-","-","-","Y","-","-","-","-","Y","-","-","-","-","-","-"]
["HUWE1","HUWE1",1,"-","-","-","-","-","-","-","-","Y","-","NA",1,14,6,"-"]
["PACS2","PACS2",1,"-","-","-","-","-","-","-","-","Y","-","NA",1,5,2,"Epileptic encephalopathy, early infantile, 66, 618067 (3), Autosomal dominant"]
["RAC1","RNASE1",1,"-","-","-","-","-","-","-","-","Y","-","NA",1,5,0,"Mental retardation, autosomal dominant 48, 617751 (3), Autosomal dominant"]
["SYT1","SYT1",1,"-","-","-","-","-","-","-","-","Y","-","NA",1,2,1,"-"]
["TAF1","TAF1",1,"-","-","-","-","-","-","-","-","Y","-","NA",1,5,0,"-"]
["ALG13","ALG13",1,"-","-","-","Y","-","-","-","-","-","-","-","-","-","-","?Congenital disorder of glycosylation, type Is, 300884 (3), X-linked dominant; Epileptic encephalopathy, early infantile, 36, 300884 (3), X-linked dominant"]
["CAMTA1","CAMTA1",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","Cerebellar ataxia, nonprogressive, with mental retardation, 614756 (3), Autosomal dominant"]
["GABRB1","GABRB1",1,"-","-","-","-","-","-","-","Y","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 45, 617153 (3), Autosomal dominant"]
["YWHAG","YWHAG",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","Epileptic encephalopathy, early infantile, 56, 617665 (3), Autosomal dominant"]
["ATP1A3","ATP1A3",1,"-","-","-","-","-","-","-","Y","-","-",3,1,13,3,"-"]
["KIF5C","KIF5C",1,"-","-","-","-","-","-","-","-","Y","-",3,1,8,3,"-"]
["NACC1","NACC1",1,"-","-","-","-","-","-","-","-","-","Y",3,1,6,1,"Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination, 617393 (3), Autosomal dominant"]
["NR2F1","NR2F1",1,"-","-","-","-","-","-","-","-","Y","-",3,1,12,5,"-"]
["SETD1B","SETD1B",1,"-","-","-","-","-","-","-","-","Y","-",3,1,9,4,"-"]
["TRRAP","TRRAP",1,"-","-","-","-","-","-","-","-","Y","-",3,1,8,3,"-"]
["ADCY3","ADCY8",1,"-","-","-","-","-","Y","-","-","-","-",2,0,2,2,"-"]
["AGO4","AGO4",1,"-","-","-","-","-","-","-","-","Y","-",2,0,3,2,"-"]
["AKAP9","AKAP9",1,"-","Y","-","-","-","-","-","-","-","-",2,0,5,4,"-"]
["APH1A","APH1A",1,"-","Y","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["ATP2B2","ATP2B4",1,"-","-","-","-","-","-","-","Y","-","-",2,0,9,8,"-"]
["CASZ1","CASZ1",1,"-","-","-","-","-","-","-","-","Y","-",2,0,4,1,"-"]
["CELF4","CELF4",1,"-","-","-","-","-","-","-","-","-","Y",2,0,10,4,"-"]
["DIP2C","DIP2C",1,"-","-","-","-","-","Y","-","-","-","-",2,0,2,1,"-"]
["DLX3","DLX3",1,"-","-","-","-","-","-","-","-","Y","-",2,0,2,1,"-"]
["DOCK8","DOCK8",1,"-","-","-","-","Y","-","-","-","-","-",2,0,10,8,"-"]
["ELAVL3","ELAVL3",1,"-","-","-","-","-","-","-","-","-","Y",2,0,3,1,"-"]
["ERBB2IP,ERBIN","ERBIN",1,"-","Y","-","-","-","-","-","-","-","-",2,0,6,6,"-"]
["ETFB","ETFB",1,"-","Y","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["GABRG3","GABRG3",1,"-","Y","-","-","-","-","-","-","-","-",2,0,9,8,"-"]
["GGNBP2","GGNBP2",1,"-","-","-","-","-","-","-","Y","-","-",2,0,2,2,"-"]
["GRIN2A","GRIN2A",1,"-","-","-","-","-","-","Y","-","-","-",2,0,39,6,"Epilepsy, focal, with speech disorder and with or without mental retardation, 245570 (3), Autosomal dominant"]
["INTS6","INTS6",1,"-","Y","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["MYO5A","MYO5A",1,"-","-","-","-","-","Y","-","-","-","-",2,0,5,5,"-"]
["NFE2L3","NFE2L3",1,"-","-","-","-","-","-","-","-","Y","-",2,0,3,2,"-"]
["NINL","NINL",1,"-","Y","-","-","-","-","-","-","-","-",2,0,6,6,"-"]
["NLGN4X,KIAA1260,NLGN4","NLGN4X",1,"-","-","-","-","-","Y","-","-","-","-",2,0,33,20,"{Asperger syndrome susceptibility, X-linked 2}, 300497 (3), X-linked; {Autism susceptibility, X-linked 2}, 300495 (3), Isolated cases, X-linked, Multifactorial; Mental retardation, X-linked, 300495 (3), Isolated cases, X-linked, Multifactorial"]
["NR3C2","NR3C2",1,"-","-","-","-","-","-","-","-","-","Y",2,1,5,5,"-"]
["OR52M1","OR52M1",1,"-","Y","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["P2RX5","P2RX5",1,"-","Y","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["PARD3B","PARD3B",1,"-","-","-","-","Y","-","-","-","-","-",2,0,7,6,"-"]
["PLXNB1","PLXNB1",1,"-","-","-","-","Y","-","-","-","-","-",2,0,3,3,"-"]
["RAB2A","RAB2A",1,"-","-","-","-","Y","-","-","-","-","-",2,0,8,5,"-"]
["RAB11B,RAB43","RAB43",1,"-","-","-","-","-","-","Y","-","-","-",2,0,2,2,"Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter, 617807 (3), Autosomal dominant"]
["SMARCA4","SMARCA4",1,"-","-","-","-","-","-","-","-","Y","-",2,0,7,3,"-"]
["SNX5","SNX5",1,"-","-","-","-","-","-","-","-","Y","-",2,0,3,2,"-"]
["SPEN","SPEN",1,"-","-","-","-","-","-","-","-","Y","-",2,0,7,4,"-"]
["TAF6","TAF6",1,"-","-","-","-","-","Y","-","-","-","-",2,0,3,3,"-"]
["USP45","USP45",1,"-","Y","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["USP7","USP7",1,"-","-","-","-","-","-","Y","-","-","-",2,1,7,4,"-"]
["WDFY4","WDFY4",1,"-","-","-","-","-","-","-","-","Y","-",2,0,6,4,"-"]
["AFF2","AFF2",1,"-","-","-","-","-","Y","-","-","-","-",1,0,15,10,"-"]
["BAZ2B","BAZ2B",1,"-","-","-","-","-","-","Y","-","-","-",1,0,4,4,"-"]
["CHD3","CHD3",1,"-","-","-","-","-","-","-","-","Y","-",1,0,6,5,"-"]
["CHD7","CHD7",1,"-","-","-","-","-","-","-","-","Y","-",1,0,28,11,"-"]
["CIC","CIC",1,"-","-","-","-","-","Y","-","-","-","-",1,0,5,3,"Mental retardation, autosomal dominant 45, 617600 (3), Autosomal dominant"]
["GIGYF2","GIGYF2",1,"-","-","-","-","Y","-","-","-","-","-",1,0,7,7,"-"]
["KCNB1","KCNB1",1,"-","-","-","-","-","-","Y","-","-","-",1,0,9,3,"Epileptic encephalopathy, early infantile, 26, 616056 (3), Autosomal dominant"]
["LZTR1","LZTR1",1,"-","-","-","-","-","-","Y","-","-","-",1,0,11,7,"-"]
["MED13","MED13",1,"-","-","-","-","-","Y","-","-","-","-",1,0,4,2,"-"]
["NR4A2","NR4A2",1,"-","-","-","-","-","-","-","-","Y","-",1,0,7,5,"-"]
["PTCHD1","PTCHD1",1,"-","-","-","-","-","-","-","-","Y","-",1,0,11,7,"{Autism, susceptibility to, X-linked 4}, 300830 (3), X-linked recessive"]
["RFX3","RFX3",1,"-","-","-","-","-","-","-","-","-","Y",1,0,6,5,"-"]
["RIMS1","RIMS1",1,"-","-","-","-","Y","-","-","-","-","-",1,0,7,5,"-"]
["RORB","RORB",1,"-","-","-","-","-","-","-","-","-","Y",1,0,5,1,"-"]
["ABI2","ABI2",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["ACTC1","ACTC1",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["ADAP1","ADAP1",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["ADCY5","ADCY5",1,"-","-","-","-","-","-","-","Y","-","-","-","-","-","-","-"]
["AGO2","AGO2",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["AGO3","AGO3",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["AP2S1","AP2S1",1,"-","-","-","-","-","-","-","-","-","Y","-","-","-","-","-"]
["AQP10","AQP10",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["ARID1A","ARID1A",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["ARIH1","ARIH1",1,"-","-","-","-","Y","-","-","-","-","-","-","-","-","-","-"]
["ASIC2","ASIC2",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["ATP8A1","ATP8A1",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["BTF3","BTN3A3",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["C2orf42","C2orf42",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["CABP7","CABP7",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["CAPN12","CAPN12",1,"-","Y","-","-","-","-","-","-","-","-","-","-","-","-","-"]
["CAPN15","CAPN15",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["CBL","CBL",1,"-","-","-","-","-","-","-","-","Y","-","-","-","-","-","-"]
["CDH10","CDH10",1,"-","-","-","-","Y","-","-","-","-","-","-","-","-","-","-"]
["CEP85L","CEP85L",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["CLDN5","CLDN5",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
["CORO1A","CORO1A",1,"-","-","-","-","-","-","-","-","-","Y","-","-","-","-","-"]
["CSNK1E","CSNK1E",1,"-","-","-","-","-","-","-","Y","-","-","-","-","-","-","-"]
["CTNND1","CTNND1",1,"-","-","-","-","-","-","Y","-","-","-","-","-","-","-","-"]
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["AP3B2","AP3B2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 48, 617276 (3), Autosomal recessive"]
["APOL2","APOL2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (1), Autosomal dominant"]
["APOL4","APOL4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (1), Autosomal dominant"]
["ARHGEF2","ARHGEF2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Neurodevelopmental disorder with midbrain and hindbrain malformations, 617523 (3), Autosomal recessive"]
["ARV1","ARV1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 38, 617020 (3), Autosomal recessive"]
["ATP6V1A","ATP6V1A",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Cutis laxa, autosomal recessive, type IID, 617403 (3), Autosomal recessive; Epileptic encephalopathy, infantile or early childhood, 3, 618012 (3), Autosomal dominant"]
["AUTS1","AUTS1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Autism susceptibility 1}, 209850 (2), Isolated cases, Multifactorial"]
["BCL11B","BCL11B",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Immunodeficiency 49, 617237 (3), Autosomal dominant; Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities, 618092 (3), Autosomal dominant"]
["BPTF","BPTF",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, 617755 (3), Autosomal dominant"]
["BRAT1","BRAT1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with cerebellar atrophy and with or without seizures, 618056 (3), Autosomal recessive; Rigidity and multifocal seizure syndrome, lethal neonatal, 614498 (3), Autosomal recessive"]
["CACNA1G","CACNA1G",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Spinocerebellar ataxia 42, 616795 (3), Autosomal dominant; Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits, 618087 (3), Autosomal dominant"]
["CACNG2","CACNG2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Mental retardation, autosomal dominant 10, 614256 (3), Autosomal dominant"]
["CCDC47","CCDC47",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Trichohepatoneurodevelopmental syndrome, 618268 (3), Autosomal recessive"]
["CDH15","CDH15",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 3, 612580 (3)"]
["CDH14","CDH18",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 3, 612580 (3)"]
["CHI3L1","CHI3L1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Asthma-related traits, susceptibility to, 7}, 611960 (3); {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["CNNM2","CNNM2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Hypomagnesemia 6, renal, 613882 (3), Autosomal dominant; Hypomagnesemia, seizures, and mental retardation, 616418 (3), Autosomal recessive, Autosomal dominant"]
["CNPY3","CNPY3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 60, 617929 (3), Autosomal recessive"]
["COMT","COMT",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Panic disorder, susceptibility to}, 167870 (3), ?Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["CPLX1","CPLX1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 63, 617976 (3), Autosomal recessive"]
["CPX1","CPXM1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 63, 617976 (3), Autosomal recessive"]
["CRADD","CRADD",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal recessive 34, with variant lissencephaly, 614499 (3), Autosomal recessive"]
["CYFIP2","CYFIP2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 65, 618008 (3), Autosomal dominant"]
["DAOA","DAOA",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["p68","DDX5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 18, 615074 (3), Autosomal dominant"]
["DENND5A","DENND5A",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 49, 617281 (3), Autosomal recessive"]
["CAD","DFFB",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 50, 616457 (3), Autosomal recessive"]
["DIP2B","DIP2B",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, FRA12A type, 136630 (3), Autosomal dominant"]
["DISC2","DISC2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Schizophrenia, 181500 (2), Autosomal dominant"]
["DOCK3","DOCK3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia, 618292 (3), Autosomal recessive"]
["DOCK7","DOCK7",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 23, 615859 (3), Autosomal recessive"]
["DPP6","DPP6",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 33, 616311 (3); {Ventricular fibrillation, paroxysmal familial, 2}, 612956 (3), Autosomal dominant"]
["DRD3","DRD3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Essential tremor, hereditary, 1}, 190300 (3), Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["ARIA","ECSCR",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{?Schizophrenia, susceptibility to}, 603013 (1)"]
["EIF4E","EIF4E",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Autism, susceptibility to, 19}, 615091 (3)"]
["ELOVL4","ELOVL4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Ichthyosis, spastic quadriplegia, and mental retardation, 614457 (3), Autosomal recessive; Spinocerebellar ataxia 34, 133190 (3), Autosomal dominant; Stargardt disease 3, 600110 (3), Autosomal dominant"]
["EPB41L1","EPB41L1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Mental retardation, autosomal dominant 11, 614257 (3), Autosomal dominant"]
["ETM1","ETM1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Essential tremor, hereditary, 1}, 190300 (3), Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["EXTL3","EXTL3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Immunoskeletal dysplasia with neurodevelopmental abnormalities, 617425 (3), Autosomal recessive"]
["FGF12","FGF12",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 47, 617166 (3), Autosomal dominant"]
["FGFR2","FGFR2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis, 207410 (3), Autosomal dominant; Apert syndrome, 101200 (3), Autosomal dominant; Beare-Stevenson cutis gyrata syndrome, 123790 (3), Autosomal dominant; Bent bone dysplasia syndrome, 614592 (3), Autosomal dominant; Craniofacial-skeletal-dermatologic dysplasia, 101600 (3), Autosomal dominant; Craniosynostosis, nonspecific (3); Crouzon syndrome, 123500 (3), Autosomal dominant; Gastric cancer, somatic, 613659 (3); Jackson-Weiss syndrome, 123150 (3), Autosomal dominant; LADD syndrome, 149730 (3), Autosomal dominant; Pfeiffer syndrome, 101600 (3), Autosomal dominant; Saethre-Chotzen syndrome, 101400 (3), Autosomal dominant; Scaphocephaly and Axenfeld-Rieger anomaly (3); Scaphocephaly, maxillary retrusion, and mental retardation, 609579 (3)"]
["FRRS1L","FRRS1L",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 37, 616981 (3), Autosomal recessive"]
["GABRA1","GABRA1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Epilepsy, childhood absence, susceptibility to, 4}, 611136 (3); {Epilepsy, juvenile myoclonic, susceptibility to, 5}, 611136 (3); Epileptic encephalopathy, early infantile, 19, 615744 (3), Autosomal dominant"]
["GATA5","GATA5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, multiple types, 5, 617912 (3), Autosomal recessive, Autosomal dominant"]
["GATA6","GATA6",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Atrial septal defect 9, 614475 (3), Autosomal dominant; Atrioventricular septal defect 5, 614474 (3), Autosomal dominant; Pancreatic agenesis and congenital heart defects, 600001 (3), Autosomal dominant; Persistent truncus arteriosus, 217095 (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant"]
["GDF1","GDF1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, multiple types, 6, 613854 (3), Autosomal dominant; Right atrial isomerism (Ivemark), 208530 (3), Autosomal recessive"]
["GDI1","GDI1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, X-linked 41, 300849 (3), X-linked dominant"]
["GEMIN4","GEMIN4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities, 617913 (3), Autosomal recessive"]
["GLS1","GLS",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 71, 618328 (3), Autosomal recessive; Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development, 618339 (3)"]
["GLS","GLS2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 71, 618328 (3), Autosomal recessive; Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development, 618339 (3)"]
["GNB1","GNB1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Leukemia, acute lymphoblastic, somatic, 613065 (3); Mental retardation, autosomal dominant 42, 616973 (3), Autosomal dominant"]
["GNB5","GNB5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Intellectual developmental disorder with cardiac arrhythmia, 617173 (3), Autosomal recessive; Language delay and ADHD/cognitive impairment with or without cardiac arrhythmia, 617182 (3), Autosomal recessive"]
["GRIA4","GRIA4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with or without seizures and gait abnormalities, 617864 (3), Autosomal dominant"]
["GRIN2D","GRIN2D",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 46, 617162 (3), Autosomal dominant"]
["GUF1","GUF1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 40, 617065 (3), Autosomal recessive"]
["HNMT","HNMT",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Asthma, susceptibility to}, 600807 (3), Autosomal dominant; Mental retardation, autosomal recessive 51, 616739 (3), Autosomal recessive"]
["HTR2A","HTR2A",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Alcohol dependence, susceptibility to}, 103780 (3), Multifactorial; {Anorexia nervosa, susceptibility to}, 606788 (3); {Major depressive disorder, response to citalopram therapy in}, 608516 (3); {Obsessive-compulsive disorder, susceptibility to}, 164230 (3), Autosomal dominant; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant; {Seasonal affective disorder, susceptibility to}, 608516 (3)"]
["IARS","IARS1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy, 617093 (3), Autosomal recessive"]
["INPP5K","INPP5K",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Muscular dystrophy, congenital, with cataracts and intellectual disability, 617404 (3), Autosomal recessive"]
["ITPA","ITPA",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 35, 616647 (3), Autosomal recessive; [Inosine triphosphatase deficiency], 613850 (3)"]
["JAG1","JAG1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Alagille syndrome 1, 118450 (3), Autosomal dominant; ?Deafness, congenital heart defects, and posterior embryotoxon, 617992 (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant"]
["KCNA2","KCNA2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 32, 616366 (3), Autosomal dominant"]
["KCNQ5","KCNQ5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 46, 617601 (3), Autosomal dominant"]
["KCNT1","KCNT1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epilepsy, nocturnal frontal lobe, 5, 615005 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 14, 614959 (3), Autosomal dominant"]
["KCNT2","KCNT2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 57, 617771 (3), Autosomal dominant"]
["KIDINS220","KIDINS220",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Spastic paraplegia, intellectual disability, nystagmus, and obesity, 617296 (3), Autosomal dominant"]
["MRX95","MAGT1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, X-linked 95, 300716 (2), X-linked dominant"]
["MDH2","MDH2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 51, 617339 (3), Autosomal recessive"]
["MRG1","MORF4L1P1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Cleft palate, cardiac defects, and mental retardation, 600987 (3), Autosomal dominant"]
["MTHFR","MTHFR",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Homocystinuria due to MTHFR deficiency, 236250 (3), Autosomal recessive; {Neural tube defects, susceptibility to}, 601634 (3), Autosomal recessive; {Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant; {Thromboembolism, susceptibility to}, 188050 (3), Autosomal dominant; {Vascular disease, susceptibility to} (3)"]
["NECAP1","NECAP1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 21, 615833 (3), Autosomal recessive"]
["NR2F2","NR2F2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, multiple types, 4, 615779 (3), Autosomal dominant"]
["NRG1","NRG1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{?Schizophrenia, susceptibility to}, 603013 (1)"]
["CFD1","NUBP2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis, 207410 (3), Autosomal dominant; Apert syndrome, 101200 (3), Autosomal dominant; Beare-Stevenson cutis gyrata syndrome, 123790 (3), Autosomal dominant; Bent bone dysplasia syndrome, 614592 (3), Autosomal dominant; Craniofacial-skeletal-dermatologic dysplasia, 101600 (3), Autosomal dominant; Craniosynostosis, nonspecific (3); Crouzon syndrome, 123500 (3), Autosomal dominant; Gastric cancer, somatic, 613659 (3); Jackson-Weiss syndrome, 123150 (3), Autosomal dominant; LADD syndrome, 149730 (3), Autosomal dominant; Pfeiffer syndrome, 101600 (3), Autosomal dominant; Saethre-Chotzen syndrome, 101400 (3), Autosomal dominant; Scaphocephaly and Axenfeld-Rieger anomaly (3); Scaphocephaly, maxillary retrusion, and mental retardation, 609579 (3)"]
["NUS1","NUS1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Congenital disorder of glycosylation, type 1aa, 617082 (3), Autosomal recessive; Mental retardation, autosomal dominant 55, with seizures, 617831 (3), Autosomal dominant"]
["OTUD6B","OTUD6B",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies, 617452 (3), Autosomal recessive"]
["CHED","OVOL2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360 (3), Autosomal dominant"]
["PHACTR1","PHACTR1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 70, 618298 (3), Autosomal dominant"]
["PIGP","PIGP",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 55, 617599 (3), Autosomal recessive"]
["ARP1","PITX2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, multiple types, 4, 615779 (3), Autosomal dominant"]
["PLAA","PLAA",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies, 617527 (3), Autosomal recessive"]
["PPP3CA","PPP3CA",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development, 618265 (3), Autosomal dominant; Epileptic encephalopathy, infantile or early childhood, 1, 617711 (3), Autosomal dominant"]
["SHS","PQBP1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3); Alpha-thalassemia/mental retardation syndrome, 301040 (3), X-linked dominant; Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3), X-linked recessive"]
["PRMT9","PRMT9",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, 618089 (3), Autosomal dominant"]
["PRODH2","PRODH2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Hyperprolinemia, type I, 239500 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 4}, 600850 (3), Autosomal dominant"]
["PRUNE1","PRUNE1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies, 617481 (3), Autosomal recessive"]
["EAP1","PTTG1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures, 618088 (3), Autosomal dominant"]
["RBM12","RBM12",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia 19, susceptibility to}, 617629 (3), Autosomal dominant"]
["SCZD9","RGS4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia 9, susceptibility to}, 604906 (3)"]
["RHOBTB2","RHOBTB2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 64, 618004 (3), Autosomal dominant"]
["RAI","RNH1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, multiple types, 6, 613854 (3), Autosomal dominant; Right atrial isomerism (Ivemark), 208530 (3), Autosomal recessive"]
["DXS648,QM","RPL10",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Autism, susceptibility to, X-linked 5}, 300847 (3); Mental retardation, X-linked, syndromic, 35, 300998 (3), X-linked recessive"]
["RPL10","RPL15",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Autism, susceptibility to, X-linked 5}, 300847 (3); Mental retardation, X-linked, syndromic, 35, 300998 (3), X-linked recessive"]
["RTN4R","RTN4R",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["SARS,SERS","SARS2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Neurodevelopmental disorder with microcephaly, ataxia, and seizures, 617709 (3), Autosomal recessive"]
["SCAPER","SCAPER",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Intellectual developmental disorder and retinitis pigmentosa, 618195 (3), Autosomal recessive"]
["SCN1B","SCN1B",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Atrial fibrillation, familial, 13, 615377 (3), Autosomal dominant; Brugada syndrome 5, 612838 (3); Cardiac conduction defect, nonspecific, 612838 (3); Epilepsy, generalized, with febrile seizures plus, type 1, 604233 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 52, 617350 (3), Autosomal recessive"]
["SCN3A","SCN3A",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epilepsy, familial focal, with variable foci 4, 617935 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 62, 617938 (3), Autosomal dominant"]
["SCZD1","SCZD1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD10","SCZD10",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia 10}, 605419 (2), Autosomal dominant"]
["SCZD2","SCZD2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{?Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD3","SCZD3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD4","SCZD4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Hyperprolinemia, type I, 239500 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 4}, 600850 (3), Autosomal dominant"]
["SCZD5","SCZD5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD6","SCZD6",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD7","SCZD7",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SCZD8","SCZD8",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia}, 181500 (2), Autosomal dominant"]
["SLC13A5","SLC13A5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 25, 615905 (3), Autosomal recessive"]
["SLC1A1","SLC1A1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Dicarboxylic aminoaciduria, 222730 (3), Autosomal recessive; {?Schizophrenia susceptibility 18}, 615232 (3)"]
["SLC25A12","SLC25A12",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 39, 612949 (3), Autosomal recessive"]
["SLC25A22","SLC25A22",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 3, 609304 (3), Autosomal recessive"]
["ATR1","SLC3A1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Alpha-thalassemia/mental retardation syndrome, type 1, 141750 (4), Autosomal dominant"]
["SLC9A9","SLC9A9",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{?Autism susceptibility 16}, 613410 (3)"]
["SOX11","SOX11",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 27, 615866 (3), Autosomal dominant"]
["SKIP","SPHKAP",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Muscular dystrophy, congenital, with cataracts and intellectual disability, 617404 (3), Autosomal recessive"]
["SPN","SPN",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Dyskinesia, seizures, and intellectual developmental disorder, 617171 (3), Autosomal recessive; Mental retardation, autosomal dominant 24, 615828 (3), Autosomal dominant"]
["SPTAN1","SPTAN1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 5, 613477 (3), Autosomal dominant"]
["SPTBN4","SPTBN4",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, 617519 (3), Autosomal recessive"]
["ST3GALII","ST3GAL2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 15, 615006 (3), Autosomal recessive; Mental retardation, autosomal recessive 12, 611090 (3), Autosomal recessive"]
["ST3GAL3","ST3GAL3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Epileptic encephalopathy, early infantile, 15, 615006 (3), Autosomal recessive; Mental retardation, autosomal recessive 12, 611090 (3), Autosomal recessive"]
["SYN2","SYN2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","{Schizophrenia, susceptibility to}, 181500 (3), Autosomal dominant"]
["SYNJ1","SYNJ1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 53, 617389 (3), Autosomal recessive; Parkinson disease 20, early-onset, 615530 (3), Autosomal recessive"]
["SZT2","SZT2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 18, 615476 (3), Autosomal recessive"]
["TBC1D24","TBC1D24",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","DOORS syndrome, 220500 (3), Autosomal recessive; Deafness , autosomal recessive 86, 614617 (3), Autosomal recessive; Deafness, autosomal dominant 65, 616044 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 16, 615338 (3), Autosomal recessive; Myoclonic epilepsy, infantile, familial, 605021 (3), Autosomal recessive"]
["TKT","TKT",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Short stature, developmental delay, and congenital heart defects, 617044 (3), Autosomal recessive"]
["TMEM94","TMEM94",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Intellectual developmental disorder with cardiac defects and dysmorphic facies, 618316 (3), Autosomal recessive"]
["TRAK1","TRAK1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 68, 618201 (3), Autosomal recessive"]
["AGS1","TREX1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Alagille syndrome 1, 118450 (3), Autosomal dominant; ?Deafness, congenital heart defects, and posterior embryotoxon, 617992 (3); Tetralogy of Fallot, 187500 (3), Autosomal dominant"]
["UBA5","UBA5",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Epileptic encephalopathy, early infantile, 44, 617132 (3), Autosomal recessive; ?Spinocerebellar ataxia, autosomal recessive 24, 617133 (3), Autosomal recessive"]
["RAD6A","UBE2A",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, X-linked syndromic, Nascimento-type, 300860 (3), X-linked recessive"]
["UFC1","UFC1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with spasticity and poor growth, 618076 (3), Autosomal recessive"]
["VARS1","VARS1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, 617802 (3), Autosomal recessive"]
["VARS2","VARS2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, 617802 (3), Autosomal recessive"]
["WARS2","WARS2",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, 617710 (3), Autosomal recessive"]
["WDPCP","WDPCP",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Bardet-Biedl syndrome 15, 615992 (3), Autosomal recessive; ?Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085 (3), Autosomal recessive"]
["WDR45B","WDR45B",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures, 617977 (3), Autosomal recessive"]
["WAGR","WT1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, 194072 (4), Autosomal dominant, Somatic mutation"]
["YAP1","YAP1",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation, 120433 (3), Autosomal dominant"]
["ZDHHC15","ZDHHC15",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","?Mental retardation, X-linked 91, 300577 (3), X-linked dominant"]
["ZIC3","ZIC3",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Congenital heart defects, nonsyndromic, 1, X-linked, 306955 (3), X-linked recessive; Heterotaxy, visceral, 1, X-linked, 306955 (3), X-linked recessive; VACTERL association, X-linked, 314390 (3), X-linked recessive"]
["MRX89","ZNF41",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, X-linked 89, 300848 (2), X-linked dominant"]
["RP58","ZNF513",0,"-","-","-","-","-","-","-","-","-","-","-","-","-","-","Mental retardation, autosomal dominant 22, 612337 (3), Autosomal dominant"]
["ANKS1B","ANKS1B",0,"-","-","-","-","-","-","-","-","-","-",3,1,3,3,"-"]
["ATP1A1","ATP1A1",0,"-","-","-","-","-","-","-","-","-","-",3,1,3,2,"Charcot-Marie-Tooth disease, axonal, type 2DD, 618036 (3), Autosomal dominant; Hypomagnesemia, seizures, and mental retardation 2, 618314 (3), Autosomal dominant"]
["CEP290","CEP290",0,"-","-","-","-","-","-","-","-","-","-",3,1,8,3,"-"]
["CHD1","CHD1",0,"-","-","-","-","-","-","-","-","-","-",3,1,4,3,"-"]
["CLCN4","CLCN4",0,"-","-","-","-","-","-","-","-","-","-",3,1,4,1,"-"]
["CUX2","CUX2",0,"-","-","-","-","-","-","-","-","-","-",3,1,8,2,"Epileptic encephalopathy, early infantile, 67, 618141 (3), Autosomal dominant"]
["DLL1","DLL1",0,"-","-","-","-","-","-","-","-","-","-",3,1,2,1,"-"]
["GABBR2","GABBR2",0,"-","-","-","-","-","-","-","-","-","-",3,1,10,2,"Epileptic encephalopathy, early infantile, 59, 617904 (3), Autosomal dominant; Neurodevelopmental disorder with poor language and loss of hand skills, 617903 (3), Autosomal dominant; {Nicotine dependence, protection against}, 188890 (3); {Nicotine dependence, susceptibility to}, 188890 (3)"]
["HDAC4","HDAC4",0,"-","-","-","-","-","-","-","-","-","-",3,1,16,3,"-"]
["MED12L","MED12L",0,"-","-","-","-","-","-","-","-","-","-",3,1,4,3,"-"]
["NFIB","NFIB",0,"-","-","-","-","-","-","-","-","-","-",3,1,5,2,"-"]
["NTNG1","NTNG1",0,"-","-","-","-","-","-","-","-","-","-",3,1,8,2,"-"]
["RNF135","RNF135",0,"-","-","-","-","-","-","-","-","-","-",3,1,4,2,"-"]
["RPS6KA3","RPS6KA3",0,"-","-","-","-","-","-","-","-","-","-",3,1,9,3,"Coffin-Lowry syndrome, 303600 (3), X-linked dominant; Mental retardation, X-linked 19, 300844 (3), X-linked dominant"]
["SYNE1","SYNE1",0,"-","-","-","-","-","-","-","-","-","-",3,1,16,9,"-"]
["TTN","TTN",0,"-","-","-","-","-","-","-","-","-","-",3,1,20,10,"-"]
["UNC13A","UNC13A",0,"-","-","-","-","-","-","-","-","-","-",3,1,6,4,"-"]
["ADA","ADA",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,5,"-"]
["AMPD1","AMPD1",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["AMT","AMT",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["ANXA1","ANXA1",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["APBB1","APBB1",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["ASAP2","ASAP2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["ASPM","ASPM",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,4,"-"]
["ASTN2","ASTN2",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,5,"-"]
["ATP10A","ATP10A",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,7,"-"]
["AVPR1A","AVPR1A",0,"-","-","-","-","-","-","-","-","-","-",2,0,22,12,"-"]
["BTAF1","BTAF1",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,7,"-"]
["CACNA1D","CACNA1D",0,"-","-","-","-","-","-","-","-","-","-",2,0,20,8,"-"]
["CACNA1H","CACNA1H",0,"-","-","-","-","-","-","-","-","-","-",2,0,27,9,"-"]
["CACNB2","CACNB2",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["CC2D1A","CC2D1A",0,"-","-","-","-","-","-","-","-","-","-",2,0,12,4,"-"]
["CCNG1","CCNG1",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["CCT4","CCT4",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["CDH13","CDH13",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["CEP135","CEP135",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,4,"-"]
["CEP41","CEP41",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,2,"-"]
["CGNL1","CGNL1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["CHMP1A","CHMP1A",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,4,"-"]
["CHRNA7","CHRNA7",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,6,"-"]
["CIB2","CIB2",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["FAM92B","CIBAR2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["CNTN4","CNTN4",0,"-","-","-","-","-","-","-","-","-","-",2,0,21,13,"-"]
["CNTN5","CNTN5",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,8,"-"]
["CNTN6","CNTN6",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,10,"-"]
["CNTNAP2","CNTNAP2",0,"-","-","-","-","-","-","-","-","-","-",2,1,67,34,"{Autism susceptibility 15}, 612100 (3); Cortical dysplasia-focal epilepsy syndrome, 610042 (3), Autosomal recessive; Pitt-Hopkins like syndrome 1, 610042 (3), Autosomal recessive"]
["CNTNAP3","CNTNAP3",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,3,"-"]
["CNTNAP4","CNTNAP4",0,"-","-","-","-","-","-","-","-","-","-",2,0,11,10,"-"]
["CPEB4","CPEB4",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["CSDE1","CSDE1",0,"-","-","-","-","-","-","-","-","-","-",2,1,2,2,"-"]
["CTNND2","CTNND2",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,3,"-"]
["CUL7","CUL7",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,6,"-"]
["CUX1","CUX1",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,3,"-"]
["CYFIP1","CYFIP1",0,"-","-","-","-","-","-","-","-","-","-",2,0,16,6,"-"]
["DAPP1","DAPP1",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["DENR","DENR",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["DISC1","DISC1",0,"-","-","-","-","-","-","-","-","-","-",2,0,34,8,"{Schizophrenia 9, susceptibility to}, 604906 (3)"]
["DLGAP1","DLGAP1",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,6,"-"]
["DPP10","DPP10",0,"-","-","-","-","-","-","-","-","-","-",2,0,11,5,"-"]
["EFR3A","EFR3A",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,5,"-"]
["ELP4","ELP4",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,6,"-"]
["EMSY","EMSY",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["EP400","EP400",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,5,"-"]
["FBN1","FBN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,10,7,"-"]
["GALNT8","GALNT8",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["GPC4","GPC4",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,1,"-"]
["GPHN","GPHN",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,4,"-"]
["GRIA1","GRIA1",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,5,"-"]
["GRID1","GRID1",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,3,"-"]
["GRIK2","GRIK2",0,"-","-","-","-","-","-","-","-","-","-",2,0,18,11,"-"]
["GRIK5","GRIK5",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,7,"-"]
["GRIN1","GRIN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,17,0,"Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant, 614254 (3), Autosomal dominant; Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive, 617820 (3), Autosomal recessive"]
["HMGN1","HMGN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["ICA1","ICA1",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,7,"-"]
["ITGB3","ITGB3",0,"-","-","-","-","-","-","-","-","-","-",2,0,15,9,"-"]
["JARID2","JARID2",0,"-","-","-","-","-","-","-","-","-","-",2,0,11,8,"-"]
["KCNJ10","KCNJ10",0,"-","-","-","-","-","-","-","-","-","-",2,0,11,4,"-"]
["KDM4C","KDM4C",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["KDM5C","KDM5C",0,"-","-","-","-","-","-","-","-","-","-",2,0,23,4,"-"]
["KIAA1586","KIAA1586",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["KIF14","KIF14",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["KIRREL3","KIRREL3",0,"-","-","-","-","-","-","-","-","-","-",2,0,15,9,"-"]
["LAMB1","LAMB1",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,7,"-"]
["LMX1B","LMX1B",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,1,"-"]
["LRP1","LRP1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["MACROD2","MACROD2",0,"-","-","-","-","-","-","-","-","-","-",2,0,19,11,"-"]
["MET","MET",0,"-","-","-","-","-","-","-","-","-","-",2,0,37,14,"-"]
["MIR137","MIR137",0,"-","-","-","-","-","-","-","-","-","-",2,0,10,2,"-"]
["DLG2","MPP2",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["MTOR","MTOR",0,"-","-","-","-","-","-","-","-","-","-",2,1,18,7,"-"]
["MYH10","MYH10",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,2,"-"]
["MYO9B","MYO9B",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["NAV2","NAV2",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,6,"-"]
["GRIP1","NCOA2",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,3,"-"]
["NCOR1","NCOR1",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,4,"-"]
["NLGN1","NLGN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,17,8,"-"]
["NUAK1","NUAK1",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,4,"-"]
["NUDCD2","NUDCD2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["OPHN1","OPHN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,15,4,"-"]
["OTUD7A","OTUD7A",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,2,"-"]
["OXTR","OXTR",0,"-","-","-","-","-","-","-","-","-","-",2,0,44,20,"-"]
["P4HA2","P4HA2",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["PAH","PAH",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,4,"-"]
["PAK2","PAK2",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,1,"-"]
["CNR1","PCDHA4",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,1,"-"]
["PER2","PER2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["PHB","PHB",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,0,"-"]
["PHRF1","PHRF1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["PLCB1","PLCB1",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,3,"Epileptic encephalopathy, early infantile, 12, 613722 (3), Autosomal recessive"]
["PLXNA4","PLXNA4",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["PON1","PON1",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,1,"-"]
["PREX1","PREX1",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["PRICKLE1","PRICKLE1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,1,"-"]
["PRICKLE2","PRICKLE2",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["PRKCB","PRKCB",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,3,"-"]
["PRKD2","PRKD2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["PRKN","PRKN",0,"-","-","-","-","-","-","-","-","-","-",2,0,15,7,"-"]
["PRODH","PRODH",0,"-","-","-","-","-","-","-","-","-","-",2,1,6,3,"Hyperprolinemia, type I, 239500 (3), Autosomal recessive; {Schizophrenia, susceptibility to, 4}, 600850 (3), Autosomal dominant"]
["PTCHD1-AS","PTCHD1-AS",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["PYHIN1","PYHIN1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["RALGAPB","RALGAPB",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["RBFOX1","RBFOX1",0,"-","-","-","-","-","-","-","-","-","-",2,0,34,9,"-"]
["RBM27","RBM27",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["ROBO2","ROBO2",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,4,"-"]
["SAE1","SAE1",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["SBF1","SBF1",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,8,"-"]
["SCN9A","SCN9A",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,2,"-"]
["SEMA5A","SEMA5A",0,"-","-","-","-","-","-","-","-","-","-",2,0,17,11,"-"]
["SHANK1","SHANK1",0,"-","-","-","-","-","-","-","-","-","-",2,0,8,6,"-"]
["SHOX","SHOX",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["SLC12A5","SLC12A5",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,2,"{Epilepsy, idiopathic generalized, susceptibility to, 14}, 616685 (3), Autosomal dominant; Epileptic encephalopathy, early infantile, 34, 616645 (3), Autosomal recessive"]
["SLC35B1","SLC35B1",0,"-","-","-","-","-","-","-","-","-","-",2,0,1,0,"-"]
["SLC38A10","SLC38A10",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,2,"-"]
["SLC6A3","SLC6A3",0,"-","-","-","-","-","-","-","-","-","-",2,0,15,5,"-"]
["SLC7A3","SLC7A3",0,"-","-","-","-","-","-","-","-","-","-",2,0,2,1,"-"]
["SLC7A5","SLC7A5",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["SLITRK5","SLITRK5",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,5,"-"]
["SPARCL1","SPARCL1",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["ST8SIA2","ST8SIA2",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,4,"-"]
["STXBP5","STXBP5",0,"-","-","-","-","-","-","-","-","-","-",2,0,6,5,"-"]
["TAOK2","TAOK2",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,3,"-"]
["TBC1D31","TBC1D31",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["TERF2","TERF2",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["TET2","TET2",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["TMLHE","TMLHE",0,"-","-","-","-","-","-","-","-","-","-",2,0,5,5,"{Autism, susceptibility to, X-linked 6}, 300872 (3), X-linked recessive"]
["TRAPPC9","TRAPPC9",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,6,"-"]
["TRPC6","TRPC6",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,2,"-"]
["TRPM1","TRPM1",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["UBE3C","UBE3C",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,4,"-"]
["UBR5","UBR5",0,"-","-","-","-","-","-","-","-","-","-",2,0,7,5,"-"]
["UNC79","UNC79",0,"-","-","-","-","-","-","-","-","-","-",2,0,4,3,"-"]
["USP15","USP15",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["VIL1","VIL1",0,"-","-","-","-","-","-","-","-","-","-",2,0,3,3,"-"]
["WWOX","WWOX",0,"-","-","-","-","-","-","-","-","-","-",2,0,9,3,"Epileptic encephalopathy, early infantile, 28, 616211 (3), Autosomal recessive; Esophageal squamous cell carcinoma, somatic, 133239 (3); Spinocerebellar ataxia, autosomal recessive 12, 614322 (3), Autosomal recessive"]
["ZNF804A","ZNF804A",0,"-","-","-","-","-","-","-","-","-","-",2,0,13,6,"-"]
["ACTB","ACTB",0,"-","-","-","-","-","-","-","-","-","-",1,0,3,1,"-"]
["ADSL","ADSL",0,"-","-","-","-","-","-","-","-","-","-",1,0,6,1,"-"]
["ALDH5A1","ALDH5A1",0,"-","-","-","-","-","-","-","-","-","-",1,0,10,3,"-"]
["ANK3","ANK3",0,"-","-","-","-","-","-","-","-","-","-",1,0,26,9,"-"]
["ARHGEF9","ARHGEF9",0,"-","-","-","-","-","-","-","-","-","-",1,0,10,4,"Epileptic encephalopathy, early infantile, 8, 300607 (3), X-linked recessive"]
["ARX","ARX",0,"-","-","-","-","-","-","-","-","-","-",1,0,17,6,"Epileptic encephalopathy, early infantile, 1, 308350 (3), X-linked recessive; Hydranencephaly with abnormal genitalia, 300215 (3), X-linked; Lissencephaly, X-linked 2, 300215 (3), X-linked; Mental retardation, X-linked 29 and others, 300419 (3), X-linked recessive; Partington syndrome, 309510 (3), X-linked recessive; Proud syndrome, 300004 (3), X-linked"]
["ATRX","ATRX",0,"-","-","-","-","-","-","-","-","-","-",1,0,21,8,"Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3); Alpha-thalassemia/mental retardation syndrome, 301040 (3), X-linked dominant; Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3), X-linked recessive"]
["BCKDK","BCKDK",0,"-","-","-","-","-","-","-","-","-","-",1,0,4,1,"-"]
["BRSK2","BRSK2",0,"-","-","-","-","-","-","-","-","-","-",1,0,4,4,"-"]
["CACNA1C","CACNA1C",0,"-","-","-","-","-","-","-","-","-","-",1,0,45,12,"-"]
["DHCR7","DHCR7",0,"-","-","-","-","-","-","-","-","-","-",1,0,17,3,"-"]
["DMPK","DMPK",0,"-","-","-","-","-","-","-","-","-","-",1,0,8,3,"-"]
["FMR1","FMR1",0,"-","-","-","-","-","-","-","-","-","-",1,0,42,7,"-"]
["HNRNPH2","HNRNPH2",0,"-","-","-","-","-","-","-","-","-","-",1,0,6,2,"Mental retardation, X-linked, syndromic, Bain type, 300986 (3), X-linked dominant"]
["HRAS","HRAS",0,"-","-","-","-","-","-","-","-","-","-",1,0,12,5,"-"]
["KDM3B","KDM3B",0,"-","-","-","-","-","-","-","-","-","-",1,0,1,0,"-"]
["MAGEL2","MAGEL2",0,"-","-","-","-","-","-","-","-","-","-",1,0,16,0,"-"]
["MBOAT7","MBOAT7",0,"-","-","-","-","-","-","-","-","-","-",1,0,6,2,"-"]
["NBEA","NBEA",0,"-","-","-","-","-","-","-","-","-","-",1,0,19,8,"-"]
["NF1","NF1",0,"-","-","-","-","-","-","-","-","-","-",1,0,24,8,"-"]
["NIPBL","NIPBL",0,"-","-","-","-","-","-","-","-","-","-",1,0,13,5,"-"]
["NLGN2","NLGN2",0,"-","-","-","-","-","-","-","-","-","-",1,0,8,4,"-"]
["NRXN2","NRXN2",0,"-","-","-","-","-","-","-","-","-","-",1,0,11,7,"-"]
["NRXN3","NRXN3",0,"-","-","-","-","-","-","-","-","-","-",1,0,18,9,"-"]
["PCDH19","PCDH19",0,"-","-","-","-","-","-","-","-","-","-",1,0,34,2,"Epileptic encephalopathy, early infantile, 9, 300088 (3), X-linked"]
["POMGNT1","POMGNT1",0,"-","-","-","-","-","-","-","-","-","-",1,0,5,3,"-"]
["PSMD12","PSMD12",0,"-","-","-","-","-","-","-","-","-","-",1,0,3,0,"-"]
["RERE","RERE",0,"-","-","-","-","-","-","-","-","-","-",1,0,7,4,"Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart, 616975 (3), Autosomal dominant"]
["SLC9A6","SLC9A6",0,"-","-","-","-","-","-","-","-","-","-",1,0,15,2,"Mental retardation, X-linked syndromic, Christianson type, 300243 (3), X-linked dominant"]
["TANC2","TANC2",0,"-","-","-","-","-","-","-","-","-","-",1,0,10,7,"-"]
["TBCK","TBCK",0,"-","-","-","-","-","-","-","-","-","-",1,0,1,0,"-"]
["TSC1","TSC1",0,"-","-","-","-","-","-","-","-","-","-",1,0,20,7,"-"]
["TSC2","TSC2",0,"-","-","-","-","-","-","-","-","-","-",1,0,30,14,"-"]
["TSHZ3","TSHZ3",0,"-","-","-","-","-","-","-","-","-","-",1,0,3,2,"-"]
["UBE3A","UBE3A",0,"-","-","-","-","-","-","-","-","-","-",1,0,27,7,"-"]
["VPS13B","VPS13B",0,"-","-","-","-","-","-","-","-","-","-",1,0,20,10,"-"]
["ZBTB20","ZBTB20",0,"-","-","-","-","-","-","-","-","-","-",1,0,22,3,"-"]
["ZNF462","ZNF462",0,"-","-","-","-","-","-","-","-","-","-",1,0,9,7,"-"]