GENENAME	GENEINFO
A2ML1	"Gene:A2ML1&HGNC:23336&OMIM:610627&UserInfo:No OMIM phenotype&UserType:SyndrRetard;NonRetardButSyndr;"
ABCC9	"Gene:ABCC9&HGNC:60&OMIM:601439&UserInfo:Atrial fibrillation, familial, 12 ; Cardiomyopathy, dilated, 1O ; Hypertrichotic osteochondrodysplasia&UserType:SyndrRetard;NonRetardButSyndr;Cardiopathy;"
ALG12	"Gene:ALG12&HGNC:19358&OMIM:607144&UserInfo:Congenital disorder of glycosylation, type Ig&UserType:SyndrRetard;Metabolism;"
CBS	"Gene:CBS&HGNC:1550&OMIM:613381&UserInfo:Homocystinuria, B6-responsive and nonresponsive types ; Thrombosis, hyperhomocysteinemic&UserType:NonSyndrRetard;SyndrRetard;Metabolism;"
COQ8A	"Gene:COQ8A&HGNC:16812&OMIM:606980&UserInfo:Coenzyme Q10 deficiency, primary, 4&UserType:NonSyndrRetard;Encephalo;Metabolism;"
DDX11	"Gene:DDX11&HGNC:2736&OMIM:601150&UserInfo:Warsaw breakage syndrome&UserType:SyndrRetard;"
HPRT1	"Gene:HPRT1&HGNC:5157&OMIM:308000&UserInfo:HPRT-related gout ; Lesch-Nyhan syndrome&UserType:NonSyndrRetard;SyndrRetard;Encephalo;Metabolism;NonRetardButSyndr;"
HRAS	"Gene:HRAS&HGNC:5173&OMIM:190020&UserInfo:Congenital myopathy with excess of muscle spindles ; Costello syndrome ; Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic ; Bladder cancer, somatic ; Nevus sebaceous or woolly hair nevus, somatic ; Spitz nevus or nevus spilus, somatic ; Thyroid carcinoma, follicular, somatic&UserType:SyndrRetard;Cardiopathy;"
NEU1	"Gene:NEU1&HGNC:7758&OMIM:608272&UserInfo:Sialidosis, type I ; Sialidosis, type II&UserType:NonSyndrRetard;SyndrRetard;Encephalo;Metabolism;"
RMRP	"Gene:RMRP&HGNC:10031&OMIM:157660&UserInfo:Anauxetic dysplasia ; Cartilage-hair hypoplasia ; Metaphyseal dysplasia without hypotrichosis&UserType:SyndrRetard;"
RNU4ATAC	"Gene:RNU4ATAC&HGNC:34016&OMIM:601428&UserInfo:Microcephalic osteodysplastic primordial dwarfism, type I ; Roifman syndrome&UserType:SyndrRetard;RetardPlusCerebAbnorm;"
SHANK2	"Gene:SHANK2&HGNC:14295&OMIM:603290&UserInfo:Autism susceptibility 17&UserType:NonSyndrRetard;"
SHANK3	"Gene:SHANK3&HGNC:14294&OMIM:606230&UserInfo:Phelan-McDermid syndrome ; Schizophrenia 15&UserType:NonSyndrRetard;"
SKI	"Gene:SKI&HGNC:10896&OMIM:164780&UserInfo:Shprintzen-Goldberg syndrome&UserType:NonSyndrRetard;"
SMS	"Gene:SMS&HGNC:11123&OMIM:300105&UserInfo:Mental retardation, X-linked, Snyder-Robinson type&UserType:SyndrRetard;"
TLK2	Gene:TLK2&HGNC:11842&OMIM:608439&UserInfo:No OMIM phenotype&UserType:
TMCO1	"Gene:TMCO1&HGNC:18188&OMIM:614123&UserInfo:Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome&UserType:SyndrRetard;"
TMLHE	"Gene:TMLHE&HGNC:18308&OMIM:300777&UserInfo:Autism, susceptibility to, X-linked 6&UserType:NonSyndrRetard;"
UBE3B	"Gene:UBE3B&HGNC:13478&OMIM:608047&UserInfo:Kaufman oculocerebrofacial syndrome&UserType:SyndrRetard;"
ZNF81	"Gene:ZNF81&HGNC:13156&OMIM:314998&UserInfo:Mental retardation, X-linked 45&UserType:NonSyndrRetard;"