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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   tourette syndrome
  

Disease ID 397
Disease tourette syndrome
Definition
A neuropsychological disorder related to alterations in DOPAMINE metabolism and neurotransmission involving frontal-subcortical neuronal circuits. Both multiple motor and one or more vocal tics need to be present with TICS occurring many times a day, nearly daily, over a period of more than one year. The onset is before age 18 and the disturbance is not due to direct physiological effects of a substance or a another medical condition. The disturbance causes marked distress or significant impairment in social, occupational, or other important areas of functioning. (From DSM-IV, 1994; Neurol Clin 1997 May;15(2):357-79)
Synonym
(psychogenic tics) or (gilles de la tourette's syndrome)
(psychogenic tics) or (gilles de la tourette's syndrome) (disorder)
chronic motor and vocal tic disorder
combined multiple motor and vocal tic disorder
combined multiple motor vocal tic dis
combined vocal and multiple motor tic disorder
combined vocal multiple motor tic dis
de gilles la tourette
de gilles la tourettes
disorder tourette
gilles de la tourette
gilles de la tourette dis
gilles de la tourette disorder
gilles de la tourette syndrome
gilles de la tourette syndrome (disorder)
gilles de la tourette's disease
gilles de la tourette's disorder
gilles de la tourette's syndr.
gilles de la tourette's syndrome
gilles de la tourette's syndrome (disorder)
gilles de la tourettes syndrome
gts
guinon's disease
maladie des tics
motor-verbal tic disorder
motor-verbal tic disorders
multiple motor and vocal tic disorder, combined
multiple motor vocal tic dis combined
psychogenic tics
syndrome gilles de la tourette
syndrome tourette
syndrome tourette's
syndrome tourettes
syndrome tourettes's
syndrome, tourette
syndromes tourette
syndromes tourettes
tic de guinon
tic dis combined vocal multiple motor
tic disorder, combined vocal and multiple motor
tourette dis
tourette disease
tourette disorder
tourette syndrome [disease/finding]
tourette's disease
tourette's disorder
tourette's disorder (disorder)
tourette's disorder -retired-
tourette's syndrome
tourette's syndrome gilles de la
tourettes dis
tourettes disease
tourettes disorder
tourettes syndrome
ts
OMIM
DOID
ICD10
UMLS
C0040517
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:15)
C1263846  |  attention deficit hyperactivity disorder  |  3
C0013384  |  dyskinesia  |  2
C0021122  |  impulse control disorders  |  1
C0851578  |  sleep disorders  |  1
C0021053  |  immune dysfunction  |  1
C0022578  |  keratoconus  |  1
C0011570  |  depression  |  1
C0037928  |  myelopathy  |  1
C0005586  |  bipolar disorder  |  1
C0004936  |  mental disorders  |  1
C0028768  |  obsessive-compulsive disorder  |  1
C0028768  |  obsessive compulsive disorder  |  1
C0040188  |  tic disorders  |  1
C0014544  |  epilepsy  |  1
C0003467  |  anxiety  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:6)
3067  |  HDC  |  CLINVAR
7298  |  TYMS  |  OMIM
2973  |  GTS  |  CTD_human
1814  |  DRD3  |  CTD_human
114798  |  SLITRK1  |  CLINVAR;CTD_human;GHR
85301  |  COL27A1  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:27)
52  |  ACP1  |  CIPHER
150  |  ADRA2A  |  CIPHER
1268  |  CNR1  |  CIPHER
1312  |  COMT  |  CIPHER
1621  |  DBH  |  CIPHER
1812  |  DRD1  |  CIPHER
1813  |  DRD2  |  CIPHER
1814  |  DRD3  |  CIPHER;CTD_human
1815  |  DRD4  |  CIPHER
2255  |  FGF10  |  CIPHER
2668  |  GDNF  |  CIPHER
348980  |  HCN1  |  CIPHER
3350  |  HTR1A  |  CIPHER
3356  |  HTR2A  |  CIPHER
3358  |  HTR2C  |  CIPHER
3587  |  IL10RA  |  CIPHER
3670  |  ISL1  |  CIPHER
3672  |  ITGA1  |  CIPHER
4128  |  MAOA  |  CIPHER
64221  |  ROBO3  |  CIPHER
54538  |  ROBO4  |  CIPHER
6507  |  SLC1A3  |  CIPHER
6531  |  SLC6A3  |  CIPHER
6532  |  SLC6A4  |  CIPHER
114798  |  SLITRK1  |  CIPHER;CTD_human
6999  |  TDO2  |  CIPHER
2973  |  GTS  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:112)
148  |  ADRA1A  |  1.969  |  DISEASES
152  |  ADRA2C  |  3.281  |  DISEASES
8227  |  AKAP17A  |  3.236  |  DISEASES
273  |  AMPH  |  1.122  |  DISEASES
9179  |  AP4M1  |  2.432  |  DISEASES
321  |  APBA2  |  1.611  |  DISEASES
54840  |  APTX  |  1.559  |  DISEASES
26053  |  AUTS2  |  2.126  |  DISEASES
627  |  BDNF  |  2.136  |  DISEASES
114781  |  BTBD9  |  3.741  |  DISEASES
79012  |  CAMKV  |  2.466  |  DISEASES
22900  |  CARD8  |  1.813  |  DISEASES
80184  |  CEP290  |  1.341  |  DISEASES
1103  |  CHAT  |  1.386  |  DISEASES
1139  |  CHRNA7  |  2.91  |  DISEASES
1268  |  CNR1  |  2.336  |  DISEASES
1272  |  CNTN1  |  1.852  |  DISEASES
6900  |  CNTN2  |  1.171  |  DISEASES
27255  |  CNTN6  |  1.694  |  DISEASES
26047  |  CNTNAP2  |  3.745  |  DISEASES
85301  |  COL27A1  |  2.47  |  DISEASES
1312  |  COMT  |  3.175  |  DISEASES
1408  |  CRY2  |  1.484  |  DISEASES
64478  |  CSMD1  |  1.822  |  DISEASES
1486  |  CTBS  |  1.962  |  DISEASES
1565  |  CYP2D6  |  1.105  |  DISEASES
1621  |  DBH  |  2.914  |  DISEASES
1804  |  DPP6  |  1.859  |  DISEASES
1812  |  DRD1  |  2.196  |  DISEASES
1813  |  DRD2  |  4.482  |  DISEASES
1814  |  DRD3  |  3.389  |  DISEASES
84062  |  DTNBP1  |  1.2  |  DISEASES
10160  |  FARP1  |  2.659  |  DISEASES
2195  |  FAT1  |  1.234  |  DISEASES
93986  |  FOXP2  |  2.133  |  DISEASES
2356  |  FPGS  |  1.838  |  DISEASES
2643  |  GCH1  |  1.883  |  DISEASES
2668  |  GDNF  |  1.094  |  DISEASES
2788  |  GNG7  |  3.153  |  DISEASES
2262  |  GPC5  |  1.981  |  DISEASES
9446  |  GSTO1  |  1.092  |  DISEASES
2996  |  GYPE  |  1.234  |  DISEASES
3127  |  HLA-DRB5  |  1.891  |  DISEASES
11255  |  HRH3  |  2.686  |  DISEASES
3351  |  HTR1B  |  1.728  |  DISEASES
3355  |  HTR1F  |  1.314  |  DISEASES
3356  |  HTR2A  |  3.591  |  DISEASES
3359  |  HTR3A  |  1.524  |  DISEASES
3363  |  HTR7  |  1.399  |  DISEASES
3064  |  HTT  |  1.585  |  DISEASES
83943  |  IMMP2L  |  5.452  |  DISEASES
102723508  |  KANTR  |  2.311  |  DISEASES
3748  |  KCNC3  |  2.004  |  DISEASES
3762  |  KCNJ5  |  1.222  |  DISEASES
114792  |  KLHL32  |  4.247  |  DISEASES
3821  |  KLRC1  |  1.157  |  DISEASES
3824  |  KLRD1  |  1.017  |  DISEASES
26468  |  LHX6  |  2.544  |  DISEASES
130574  |  LYPD6  |  3.479  |  DISEASES
4094  |  MAF  |  1.582  |  DISEASES
4128  |  MAOA  |  2.664  |  DISEASES
4129  |  MAOB  |  1.178  |  DISEASES
115004  |  MB21D1  |  2.509  |  DISEASES
4204  |  MECP2  |  1.198  |  DISEASES
4340  |  MOG  |  1.018  |  DISEASES
4697  |  NDUFA4  |  2.725  |  DISEASES
9520  |  NPEPPS  |  1.388  |  DISEASES
4897  |  NRCAM  |  1.523  |  DISEASES
9378  |  NRXN1  |  3.672  |  DISEASES
59277  |  NTN4  |  2.448  |  DISEASES
266553  |  OFCC1  |  4.91  |  DISEASES
116448  |  OLIG1  |  2.061  |  DISEASES
10215  |  OLIG2  |  1.068  |  DISEASES
27328  |  PCDH11X  |  2.021  |  DISEASES
359809  |  PEG13  |  3.344  |  DISEASES
8301  |  PICALM  |  1.229  |  DISEASES
11128  |  POLR3A  |  3.487  |  DISEASES
728378  |  POTEF  |  1.349  |  DISEASES
144165  |  PRICKLE1  |  2.333  |  DISEASES
5631  |  PRPS1  |  1.804  |  DISEASES
221823  |  PRPS1L1  |  2.296  |  DISEASES
112476  |  PRRT2  |  1.17  |  DISEASES
5646  |  PRSS3  |  1.096  |  DISEASES
5789  |  PTPRD  |  1.488  |  DISEASES
1104  |  RCC1  |  1.723  |  DISEASES
391  |  RHOG  |  2.045  |  DISEASES
253260  |  RICTOR  |  1.071  |  DISEASES
64221  |  ROBO3  |  1.912  |  DISEASES
57142  |  RTN4  |  3.861  |  DISEASES
8910  |  SGCE  |  3.499  |  DISEASES
390598  |  SKOR1  |  2.531  |  DISEASES
57282  |  SLC4A10  |  2.743  |  DISEASES
6586  |  SLIT3  |  1.335  |  DISEASES
114798  |  SLITRK1  |  5.619  |  DISEASES
84631  |  SLITRK2  |  3.346  |  DISEASES
139065  |  SLITRK4  |  3.354  |  DISEASES
26050  |  SLITRK5  |  2.951  |  DISEASES
134957  |  STXBP5  |  2.689  |  DISEASES
64420  |  SUSD1  |  4.499  |  DISEASES
136306  |  SVOPL  |  4.068  |  DISEASES
51256  |  TBC1D7  |  1.32  |  DISEASES
6904  |  TBCD  |  3.283  |  DISEASES
6999  |  TDO2  |  4.207  |  DISEASES
55775  |  TDP1  |  1.846  |  DISEASES
1861  |  TOR1A  |  1.11  |  DISEASES
9760  |  TOX  |  1.187  |  DISEASES
121278  |  TPH2  |  1.713  |  DISEASES
83696  |  TRAPPC9  |  2.161  |  DISEASES
9960  |  USP3  |  3.456  |  DISEASES
23230  |  VPS13A  |  1.659  |  DISEASES
55112  |  WDR60  |  2.998  |  DISEASES
23286  |  WWC1  |  2.125  |  DISEASES
Locus(Waiting for update.)
Disease ID 397
Disease tourette syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:23)
HP:0100033  |  Tic disorder  |  34
HP:0000752  |  Hyperactive behavior  |  5
HP:0100034  |  Motor tics  |  3
HP:0007018  |  Attention deficits  |  3
HP:0100660  |  Dyskinesis  |  2
HP:0000708  |  Behavioral problems  |  2
HP:0100035  |  Vocal tics  |  2
HP:0000722  |  Obsessive compulsive disorder  |  2
HP:0100022  |  Movement disorder  |  1
HP:0000739  |  Anxiety  |  1
HP:0000734  |  Disinhibition  |  1
HP:0011468  |  Facial tics  |  1
HP:0002318  |  Cervical myelopathy  |  1
HP:0002930  |  Resistance to thyroid hormone  |  1
HP:0002196  |  Myelopathy  |  1
HP:0000563  |  Conical cornea  |  1
HP:0100716  |  Autoagression  |  1
HP:0001631  |  Atria septal defect  |  1
HP:0040141  |  Tardive dyskinesia  |  1
HP:0000716  |  Depression  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0002315  |  Headaches  |  1
HP:0000473  |  Spasmodic torticollis  |  1
Disease ID 397
Disease tourette syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0149645  |  cervical myelopathy  |  1
C0751900  |  motor tics  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:21)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10590041728328810215OLIG2umls:C0040517BeFreeThe following 3 single nucleotide polymorphism markers on OLIG2 were associated with the OCD without TD phenotype: rs762178 (minor allele frequency, 35%; P<.001), rs1059004 (minor allele frequency, 44%; P = .005), and rs9653711 (minor allele frequency, 44%; P = .004).0.0002714422007OLIG22133028155CA
rs191284403NA114798SLITRK1umls:C0040517CLINVARNA0.347161507NASLITRK11383878728CT
rs193302861NA114798SLITRK1umls:C0040517CLINVARNA0.347161507NASLITRK11383880244G-
rs267606861NA3067HDCumls:C0040517CLINVARNA0.200814326NAHDC1550252520CT
rs386602276200104503350HTR1Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0026384742010NANANANANA
rs386602276200104506532SLC6A4umls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010NANANANANA
rs386602276200104503356HTR2Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010NANANANANA
rs386602280200104503356HTR2Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010NANANANANA
rs386602280200104503350HTR1Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0026384742010NANANANANA
rs386602280200104506532SLC6A4umls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010NANANANANA
rs6280256981991814DRD3umls:C0040517BeFreeAssociation between Tourette syndrome and the dopamine D3 receptor gene rs6280.0.125548392015DRD33114171968CT
rs6295200104506532SLC6A4umls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010HTR1A563962738CG
rs6295200104503350HTR1Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0026384742010HTR1A563962738CG
rs6295200104503356HTR2Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010HTR1A563962738CG
rs6311172418283356HTR2Aumls:C0040517BeFreeNominally significant association was found at the HTR2A rs6311 polymorphism in subjects with tic disorder and OCD (p = .05), replicating a previous finding in Tourette syndrome and OCD.0.0052769482007HTR2A1346897343CT
rs6313200104503350HTR1Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0026384742010HTR2A1346895805GA
rs6313200104503356HTR2Aumls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010HTR2A1346895805GA
rs6313200104506532SLC6A4umls:C0040517BeFreeAs neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.0.0052769482010HTR2A1346895805GA
rs7621781728328810215OLIG2umls:C0040517BeFreeThe following 3 single nucleotide polymorphism markers on OLIG2 were associated with the OCD without TD phenotype: rs762178 (minor allele frequency, 35%; P<.001), rs1059004 (minor allele frequency, 44%; P = .005), and rs9653711 (minor allele frequency, 44%; P = .004).0.0002714422007OLIG22133027093AG
rs78689922288992485301COL27A1umls:C0040517GWASCATGenome-wide association study of Tourette's syndrome.0.122014COL27A19114228791GA
rs96537111728328810215OLIG2umls:C0040517BeFreeThe following 3 single nucleotide polymorphism markers on OLIG2 were associated with the OCD without TD phenotype: rs762178 (minor allele frequency, 35%; P<.001), rs1059004 (minor allele frequency, 44%; P = .005), and rs9653711 (minor allele frequency, 44%; P = .004).0.0002714422007OLIG22133029641GC
GWASdb Annotation(Total Genotypes:5)
Chr Pos SNP_Id RefGene EnsemblGene ENCODE_Factor ENCODE_TFBS Chromosome_interaction GTEx_eQTL SNP_TFBS_affinity_GWAS3D SNP_miRNA_target_affinity_PolymiRTS SNP_splicing_effect_Skippy SNP_splicing_effect_MutPred_Splice SNP_ns_protein_effect_dbNSFP SNP_syn_effect_Silva SNP_phosphorylation_effect_PhosSNP PhastCons_score PhyloP_score GERP++_RS Segway_state Ancestral_allele ESP_AF ESP_AFR ESP_AFR ESP_EUR TG_ASN TG_AMR TG_AFR TG_EUR Type Consequence bStatistic EncH3K27Ac EncH3K4Me1 EncH3K4Me3 EncNucleo OMIM Clinvar
18659236rs502396NM_001012716,C18orf56NM_001071,TYMSENST00000323813,ENSG00000176912ENST00000323274,ENSG00000176890ENST00000323224,ENSG00000176890ENST00000323250,ENSG00000176890TFP.MAXTFP.MAFFTFP.MAFKMCV-9NANANAYpr015c-primary,2.3383Ypr196w-primary,1.87Yrm1-primary,3.5637Yrm1-primary,2.8431LM12,7.5746NANANANANANA0.000-1.375-6.3E/GMTNANANANANANA
18659829rs2853539NM_001071,TYMSENST00000323274,ENSG00000176890ENST00000323224,ENSG00000176890ENST00000323250,ENSG00000176890NANANANACep3-primary,1.3137Cep3-primary,1.7522Cha4-primary,9.1892Dmbx1_2277,1.8362Mcm1-primary,2.7369NANANANANANA0.066-0.147-0.537GM1ANANANANANANANANAIntergenicUPSTREAM878
18661005rs2244500NM_001071,TYMSENST00000323274,ENSG00000176890ENST00000323224,ENSG00000176890ENST00000323250,ENSG00000176890NANAchr18,660001,670000,chr18,9050001,9060000,6,Hi-CNAEmx2_3420,1.3964Evx1_3952,1.5693Gbx1_2883,1.6994Gbx2_3110,1.514Lhx4_1719,2.1456NANANANANANA0.001-0.122-0.481GE1GNANANANANANANANAIntergenicUPSTREAM861
18661647rs2847153NM_001071,TYMSENST00000323274,ENSG00000176890ENST00000323224,ENSG00000176890ENST00000323250,ENSG00000176890NANAchr18,660001,670000,chr18,9050001,9060000,6,Hi-CNADmbx1_2277,1.53Dobox5_3493,1.4078Gsc_2327,1.3787Hoxc10_2779,7.7287Obox1_3970,1.3032NANANANANANA0.000-0.972-3.73GE2GNANANA0.2700.4000.2000.2800.200IntergenicUPSTREAM850
18662135rs11873890NM_001071,TYMSENST00000323274,ENSG00000176890ENST00000323224,ENSG00000176890ENST00000323250,ENSG00000176890MCV-7TFP.JUNBNAchr18,660001,670000,chr18,9050001,9060000,6,Hi-CNAMZF1,2.0077STAT1,1.3513STAT1,3.489Pax-9,1.7445STAT,2.9053NANANANANANA0.000-4.042-10.9GE2ANANANANANANANANAIntergenicUPSTREAM
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 397
Disease tourette syndrome
Case(Waiting for update.)