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Pediatric Disease Annotations & Medicines



   tic disorder
  

Disease ID 854
Disease tic disorder
Definition
Disorders characterized by recurrent TICS that may interfere with speech and other activities. Tics are sudden, rapid, nonrhythmic, stereotyped motor movements or vocalizations which may be exacerbated by stress and are generally attenuated during absorbing activities. Tic disorders are distinguished from conditions which feature other types of abnormal movements that may accompany another another condition. (From DSM-IV, 1994)
Synonym
[x]tic disorders
[x]tic disorders (finding)
disorders habit
habit disorder
tic
tic (finding)
tic [dup] (finding)
tic dis
tic disorder (disorder)
tic disorder nos
tic disorder unspecified
tic disorder unspecified (disorder)
tic disorder unspecified (finding)
tic disorder, nos
tic disorder, unspecified
tic disorders
tic disorders [disease/finding]
tic nos
tic nos (finding)
tic, nos
tics
OMIM
DOID
ICD10
UMLS
C0040188
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:275)
C0036341  |  schizophrenia  |  20
C0025362  |  mental retardation  |  14
C0039730  |  thalassemia  |  11
C0011847  |  diabetes  |  10
C0004352  |  autism  |  8
C0679466  |  cognitive deficits  |  7
C0003467  |  anxiety  |  7
C0011570  |  depression  |  7
C0033975  |  psychosis  |  6
C0014544  |  epilepsy  |  6
C0497327  |  dementia  |  5
C0021053  |  immune disease  |  5
C0028754  |  obesity  |  5
C0020538  |  hypertension  |  5
C0005586  |  bipolar disorder  |  5
C0028768  |  obsessive-compulsive disorder  |  4
C0023895  |  liver disease  |  4
C0010674  |  cystic fibrosis  |  4
C0002871  |  anemia  |  4
C0023890  |  cirrhosis  |  4
C0040034  |  thrombocytopenia  |  4
C0030312  |  bone marrow failure  |  4
C0035078  |  renal failure  |  4
C0022658  |  kidney disease  |  3
C0022661  |  end-stage renal failure  |  3
C0018799  |  heart disease  |  3
C0029408  |  osteoarthritis  |  3
C0001125  |  lactic acidosis  |  3
C0751651  |  mitochondrial disease  |  3
C0020542  |  pulmonary hypertension  |  3
C0040053  |  thrombosis  |  3
C0019045  |  hemoglobinopathies  |  3
C0282193  |  iron overload  |  3
C0022658  |  renal disease  |  3
C0242379  |  lung cancer  |  3
C0031106  |  aggressive periodontitis  |  2
C0033953  |  sexual dysfunction  |  2
C0026850  |  muscular dystrophies  |  2
C0004936  |  mental disorders  |  2
C0016667  |  fragile x syndrome  |  2
C0085113  |  neurofibromatosis  |  2
C0751651  |  mitochondrial diseases  |  2
C0030486  |  paraplegia  |  2
C0001627  |  congenital adrenal hyperplasia  |  2
C0002020  |  alexithymia  |  2
C0476089  |  endometrial cancer  |  2
C0019158  |  hepatitis  |  2
C0023890  |  liver cirrhosis  |  2
C0040100  |  thymoma  |  2
C0022661  |  chronic kidney disease  |  2
C0017920  |  g6pd deficiency  |  2
C0011860  |  type 2 diabetes  |  2
C0018995  |  hemochromatosis  |  2
C0033975  |  psychoses  |  2
C0041696  |  major depressive disorder  |  2
C0038436  |  post-traumatic stress disorder  |  2
C0021053  |  immune disorder  |  2
C0024530  |  malaria  |  2
C0004153  |  atherosclerosis  |  2
C0035078  |  kidney failure  |  2
C0856761  |  budd-chiari syndrome  |  2
C0021053  |  immune disorders  |  2
C0031099  |  periodontitis  |  2
C0085413  |  autosomal dominant polycystic kidney disease  |  2
C0948265  |  metabolic syndrome  |  2
C0751265  |  learning disabilities  |  2
C0018552  |  hamartomas  |  2
C0024299  |  lymphoma  |  2
C0038436  |  posttraumatic stress disorder  |  2
C0002871  |  anaemia  |  2
C0476089  |  endometrial ca  |  2
C0022578  |  keratoconus  |  2
C0017601  |  glaucoma  |  2
C0018801  |  heart failure  |  2
C1621895  |  adrenal hyperplasia  |  2
C0027121  |  myositis  |  2
C0010068  |  coronary artery disease  |  2
C1136084  |  plasma cell dyscrasia  |  2
C0699893  |  nonmelanoma skin cancer  |  1
C0026691  |  kawasaki disease  |  1
C0002895  |  sickle cell anaemia  |  1
C0206728  |  plexiform neurofibroma  |  1
C0007361  |  cat scratch disease  |  1
C0026986  |  myelodysplastic syndromes  |  1
C0020443  |  hypercholesterolaemia  |  1
C0020437  |  hypercalcaemia  |  1
C0037280  |  infestation  |  1
C0033626  |  protein deficiency  |  1
C0023895  |  hepatic disease  |  1
C0013473  |  eating disorders  |  1
C0013080  |  trisomy 21  |  1
C0027859  |  vestibular schwannomas  |  1
C0010403  |  cryoglobulinaemia  |  1
C0014859  |  esophageal cancer  |  1
C0403447  |  chronic renal insufficiency  |  1
C0027765  |  nervous system disease  |  1
C0003499  |  supravalvular aortic stenosis  |  1
C0020445  |  familial hypercholesterolemia  |  1
C0158266  |  disc degeneration  |  1
C0013421  |  dystonia  |  1
C0018021  |  goiter  |  1
C0271097  |  usher syndrome  |  1
C0031511  |  pheochromocytomas  |  1
C0031212  |  personality disorders  |  1
C0020541  |  portal hypertension  |  1
C0031117  |  peripheral neuropathy  |  1
C0022661  |  chronic renal failure  |  1
C0017205  |  gaucher's disease  |  1
C0018802  |  congestive heart failure  |  1
C0040128  |  thyroid disorders  |  1
C0149925  |  small cell lung cancer  |  1
C0025958  |  microcephaly  |  1
C0041408  |  turner syndrome  |  1
C0013720  |  ehlers-danlos syndrome  |  1
C0006840  |  candida infection  |  1
C0159069  |  impaired glucose tolerance  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0014544  |  epileptic seizure  |  1
C0878544  |  cardiomyopathies  |  1
C0376358  |  prostate cancer  |  1
C0022661  |  end stage renal disease  |  1
C0079924  |  oligohydramnios  |  1
C0023470  |  myeloid leukemia  |  1
C0007114  |  skin cancers  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C0027873  |  neuromyelitis optica  |  1
C0031090  |  periodontal diseases  |  1
C0042373  |  vascular disease  |  1
C0022661  |  end stage renal disease (esrd)  |  1
C0030305  |  pancreatitis  |  1
C0158683  |  polycystic liver disease  |  1
C0042384  |  vasculitis  |  1
C0007114  |  skin cancer  |  1
C0019069  |  hemophilia  |  1
C0085078  |  lysosomal storage disease  |  1
C0010068  |  coronary heart disease  |  1
C0751882  |  congenital myasthenic syndrome  |  1
C0030567  |  parkinson's disease  |  1
C0041341  |  tuberous sclerosis  |  1
C0028768  |  obsessive compulsive disorder  |  1
C0002871  |  anemias  |  1
C0032580  |  familial adenomatous polyposis  |  1
C0003864  |  arthritis  |  1
C0153398  |  hypopharyngeal cancer  |  1
C0036439  |  scoliosis  |  1
C0878544  |  cardiomyopathy  |  1
C0021359  |  infertility  |  1
C0221757  |  aat deficiency  |  1
C0022972  |  myasthenic syndrome  |  1
C0235522  |  venous disease  |  1
C0011854  |  type 1 diabetes  |  1
C0018799  |  cardiac disease  |  1
C0747256  |  parasitic infection  |  1
C0011644  |  scleroderma  |  1
C0027859  |  vestibular schwannoma  |  1
C0022735  |  klinefelter syndrome  |  1
C0349464  |  korsakoff syndrome  |  1
C0003469  |  anxiety disorder  |  1
C0853193  |  bipolar i disorder  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0035921  |  congenital rubella syndrome  |  1
C0002878  |  hemolytic anemia  |  1
C0014544  |  seizure disorder  |  1
C0026764  |  myeloma  |  1
C0003507  |  aortic stenosis  |  1
C0035921  |  congenital rubella  |  1
C0020445  |  familial hypercholesterolaemia  |  1
C0022104  |  irritable bowel syndrome  |  1
C0022661  |  end-stage renal disease  |  1
C0003635  |  apraxia  |  1
C0271650  |  glucose intolerance  |  1
C0221355  |  macrocephaly  |  1
C0175702  |  williams-beuren syndrome  |  1
C0003507  |  valvular aortic stenosis  |  1
C0020757  |  icthyosis  |  1
C0019618  |  histiocytosis  |  1
C0020635  |  hypopituitarism  |  1
C0005586  |  bipolar affective disorder  |  1
C0002895  |  sickle cell anemia  |  1
C0013473  |  eating disorder  |  1
C0024117  |  chronic obstructive pulmonary disease  |  1
C0031090  |  periodontal disease  |  1
C0010278  |  craniosynostosis  |  1
C0014544  |  epileptic seizures  |  1
C0032371  |  polio  |  1
C0027051  |  myocardial infarction (mi)  |  1
C0020492  |  hyperostosis  |  1
C0268483  |  tyrosinemia  |  1
C0004134  |  ataxia  |  1
C0748023  |  bacterial prostatitis  |  1
C0020555  |  hypertrichosis  |  1
C0004509  |  azoospermia  |  1
C0015397  |  ocular disease  |  1
C0040188  |  tic disorders  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0011849  |  diabetes mellitus  |  1
C0039446  |  telangiectases  |  1
C0241910  |  autoimmune hepatitis  |  1
C0007570  |  celiac disease  |  1
C0035372  |  rett syndrome  |  1
C0025286  |  meningiomas  |  1
C0026703  |  mucopolysaccharidoses  |  1
C0152021  |  congenital heart disease  |  1
C0026393  |  molluscum contagiosum  |  1
C0751651  |  mitochondrial disorders  |  1
C0221023  |  cyclic neutropenia  |  1
C0851578  |  sleep disorders  |  1
C0392525  |  nephrolithiasis  |  1
C0006840  |  candida infections  |  1
C0039730  |  thalassaemia  |  1
C0035435  |  rheumatism  |  1
C0035333  |  retinitis  |  1
C0002312  |  alpha thalassemia  |  1
C0020443  |  hypercholesterolemia  |  1
C0280131  |  ovarian teratoma  |  1
C0035304  |  retinal degeneration  |  1
C0004943  |  behcet's disease  |  1
C0023467  |  acute myeloid leukemia  |  1
C0024117  |  chronic obstructive pulmonary disease (copd)  |  1
C1565489  |  renal insufficiency  |  1
C0020598  |  hypoglycaemia  |  1
C0149931  |  migraine  |  1
C0022661  |  chronic renal disease  |  1
C0027765  |  nervous system diseases  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0002395  |  senile dementia  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0035920  |  rubella  |  1
C0030326  |  panniculitis  |  1
C0154246  |  urea cycle disorders  |  1
C0020456  |  hyperglycaemia  |  1
C0085576  |  microcytic anemia  |  1
C0037317  |  sleep disturbances  |  1
C0013384  |  dyskinesia  |  1
C0033581  |  prostatitis  |  1
C0162839  |  porokeratosis  |  1
C0002895  |  sickle cell disease  |  1
C0011265  |  presenile dementia  |  1
C0039538  |  teratomas  |  1
C0020544  |  renal hypertension  |  1
C0040053  |  thrombus  |  1
C0014556  |  temporal lobe epilepsy  |  1
C1263846  |  attention deficit hyperactivity disorder  |  1
C0027830  |  neurofibromas  |  1
C0020179  |  huntington disease  |  1
C0751651  |  mitochondrial disorder  |  1
C0003469  |  anxiety disorders  |  1
C0007570  |  coeliac disease  |  1
C0032580  |  adenomatous polyposis  |  1
C0028768  |  obsessive-compulsive disorders  |  1
C0003873  |  rheumatoid arthritis  |  1
C0042974  |  von willebrand disease  |  1
C0037317  |  sleep disturbance  |  1
C0271270  |  oculomotor apraxia  |  1
C0546837  |  oesophageal cancer  |  1
C0011860  |  type 2 diabetes mellitus  |  1
C0476089  |  endometrial cancers  |  1
C0026764  |  multiple myeloma  |  1
C0033687  |  proteinuria  |  1
C0014544  |  epilepsies  |  1
C0031347  |  pharyngeal cancer  |  1
C0020474  |  familial combined hyperlipidemia  |  1
C0001430  |  adenoma  |  1
C0085293  |  hepatitis e  |  1
C0456909  |  blindness  |  1
C0162309  |  adrenoleukodystrophy  |  1
C0035334  |  retinitis pigmentosa  |  1
C0027947  |  neutropenia  |  1
C0023891  |  alcoholic cirrhosis  |  1
C0236792  |  asperger syndrome  |  1
C0023646  |  lichen planus  |  1
C0206728  |  plexiform neurofibromas  |  1
C0036337  |  schizoaffective disorder  |  1
C0085078  |  lysosomal storage diseases  |  1
C0008370  |  cholestasis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:4)
DRD4  |  1815  |  CTD_human
SLITRK1  |  114798  |  GHR
PSD4  |  23550  |  OMIM
SLC6A3  |  6531  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:216)
1951  |  CELSR3  |  DISEASES
1815  |  DRD4  |  DISEASES
5607  |  MAP2K5  |  DISEASES
6820  |  SULT2B1  |  DISEASES
5816  |  PVALB  |  DISEASES
10278  |  EFS  |  DISEASES
6530  |  SLC6A2  |  DISEASES
83988  |  NCALD  |  DISEASES
6449  |  SGTA  |  DISEASES
4818  |  NKG7  |  DISEASES
7431  |  VIM  |  DISEASES
969  |  CD69  |  DISEASES
81491  |  GPR63  |  DISEASES
13  |  AADAC  |  DISEASES
9168  |  TMSB10  |  DISEASES
58512  |  DLGAP3  |  DISEASES
9409  |  PEX16  |  DISEASES
56269  |  IRGC  |  DISEASES
53947  |  A4GALT  |  DISEASES
10439  |  OLFM1  |  DISEASES
51659  |  GINS2  |  DISEASES
2161  |  F12  |  DISEASES
3337  |  DNAJB1  |  DISEASES
6616  |  SNAP25  |  DISEASES
1455  |  CSNK1G2  |  DISEASES
78986  |  DUSP26  |  DISEASES
1022  |  CDK7  |  DISEASES
3357  |  HTR2B  |  DISEASES
51133  |  KCTD3  |  DISEASES
3557  |  IL1RN  |  DISEASES
29113  |  C6orf15  |  DISEASES
9177  |  HTR3B  |  DISEASES
10017  |  BCL2L10  |  DISEASES
23317  |  DNAJC13  |  DISEASES
1295  |  COL8A1  |  DISEASES
6532  |  SLC6A4  |  DISEASES
6505  |  SLC1A1  |  DISEASES
7515  |  XRCC1  |  DISEASES
57084  |  SLC17A6  |  DISEASES
2033  |  EP300  |  DISEASES
56925  |  LXN  |  DISEASES
2557  |  GABRA4  |  DISEASES
2891  |  GRIA2  |  DISEASES
119  |  ADD2  |  DISEASES
2255  |  FGF10  |  DISEASES
11222  |  MRPL3  |  DISEASES
6507  |  SLC1A3  |  DISEASES
2568  |  GABRP  |  DISEASES
1181  |  CLCN2  |  DISEASES
6585  |  SLIT1  |  DISEASES
3067  |  HDC  |  DISEASES
1000  |  CDH2  |  DISEASES
409  |  ARRB2  |  DISEASES
147381  |  CBLN2  |  DISEASES
6531  |  SLC6A3  |  DISEASES
52  |  ACP1  |  DISEASES
4211  |  MEIS1  |  DISEASES
6581  |  SLC22A3  |  DISEASES
57502  |  NLGN4X  |  DISEASES
3358  |  HTR2C  |  DISEASES
3145  |  HMBS  |  DISEASES
3176  |  HNMT  |  DISEASES
150  |  ADRA2A  |  DISEASES
25836  |  NIPBL  |  DISEASES
3672  |  ITGA1  |  DISEASES
3192  |  HNRNPU  |  DISEASES
23522  |  KAT6B  |  DISEASES
3361  |  HTR5A  |  DISEASES
9437  |  NCR1  |  DISEASES
3060  |  HCRT  |  DISEASES
9965  |  FGF19  |  DISEASES
431707  |  LHX8  |  DISEASES
2565  |  GABRG1  |  DISEASES
85477  |  SCIN  |  DISEASES
6571  |  SLC18A2  |  DISEASES
3251  |  HPRT1  |  DISEASES
2562  |  GABRB3  |  DISEASES
89832  |  CHRFAM7A  |  DISEASES
5479  |  PPIB  |  DISEASES
5347  |  PLK1  |  DISEASES
10982  |  MAPRE2  |  DISEASES
6632  |  SNRPD1  |  DISEASES
51305  |  KCNK9  |  DISEASES
6249  |  CLIP1  |  DISEASES
54538  |  ROBO4  |  DISEASES
53407  |  STX18  |  DISEASES
7399  |  USH2A  |  DISEASES
1816  |  DRD5  |  DISEASES
2243  |  FGA  |  DISEASES
255239  |  ANKK1  |  DISEASES
219833  |  C11orf45  |  DISEASES
140886  |  PABPC5  |  DISEASES
134  |  ADORA1  |  DISEASES
54715  |  RBFOX1  |  DISEASES
5707  |  PSMD1  |  DISEASES
1808  |  DPYSL2  |  DISEASES
56945  |  MRPS22  |  DISEASES
80025  |  PANK2  |  DISEASES
3352  |  HTR1D  |  DISEASES
6844  |  VAMP2  |  DISEASES
3350  |  HTR1A  |  DISEASES
9520  |  NPEPPS  |  DISEASES
134957  |  STXBP5  |  DISEASES
3355  |  HTR1F  |  DISEASES
10160  |  FARP1  |  DISEASES
8227  |  AKAP17A  |  DISEASES
1272  |  CNTN1  |  DISEASES
4094  |  MAF  |  DISEASES
1812  |  DRD1  |  DISEASES
121278  |  TPH2  |  DISEASES
83943  |  IMMP2L  |  DISEASES
6900  |  CNTN2  |  DISEASES
10215  |  OLIG2  |  DISEASES
5813  |  PURA  |  DISEASES
130574  |  LYPD6  |  DISEASES
139065  |  SLITRK4  |  DISEASES
1103  |  CHAT  |  DISEASES
55775  |  TDP1  |  DISEASES
57142  |  RTN4  |  DISEASES
3363  |  HTR7  |  DISEASES
391  |  RHOG  |  DISEASES
4697  |  NDUFA4  |  DISEASES
3762  |  KCNJ5  |  DISEASES
4128  |  MAOA  |  DISEASES
59277  |  NTN4  |  DISEASES
84062  |  DTNBP1  |  DISEASES
27255  |  CNTN6  |  DISEASES
11255  |  HRH3  |  DISEASES
26053  |  AUTS2  |  DISEASES
144165  |  PRICKLE1  |  DISEASES
1861  |  TOR1A  |  DISEASES
3064  |  HTT  |  DISEASES
6904  |  TBCD  |  DISEASES
3359  |  HTR3A  |  DISEASES
85301  |  COL27A1  |  DISEASES
273  |  AMPH  |  DISEASES
5789  |  PTPRD  |  DISEASES
51256  |  TBC1D7  |  DISEASES
253260  |  RICTOR  |  DISEASES
728378  |  POTEF  |  DISEASES
2996  |  GYPE  |  DISEASES
112476  |  PRRT2  |  DISEASES
3821  |  KLRC1  |  DISEASES
9179  |  AP4M1  |  DISEASES
23230  |  VPS13A  |  DISEASES
1565  |  CYP2D6  |  DISEASES
5646  |  PRSS3  |  DISEASES
1312  |  COMT  |  DISEASES
26047  |  CNTNAP2  |  DISEASES
9760  |  TOX  |  DISEASES
1813  |  DRD2  |  DISEASES
114792  |  KLHL32  |  DISEASES
1268  |  CNR1  |  DISEASES
9446  |  GSTO1  |  DISEASES
3351  |  HTR1B  |  DISEASES
115004  |  MB21D1  |  DISEASES
84631  |  SLITRK2  |  DISEASES
1486  |  CTBS  |  DISEASES
11128  |  POLR3A  |  DISEASES
5631  |  PRPS1  |  DISEASES
27328  |  PCDH11X  |  DISEASES
2356  |  FPGS  |  DISEASES
3061  |  HCRTR1  |  DISEASES
1104  |  RCC1  |  DISEASES
64420  |  SUSD1  |  DISEASES
3127  |  HLA-DRB5  |  DISEASES
267012  |  DAOA  |  DISEASES
2262  |  GPC5  |  DISEASES
26050  |  SLITRK5  |  DISEASES
114798  |  SLITRK1  |  DISEASES
1804  |  DPP6  |  DISEASES
4129  |  MAOB  |  DISEASES
3356  |  HTR2A  |  DISEASES
4897  |  NRCAM  |  DISEASES
54840  |  APTX  |  DISEASES
390598  |  SKOR1  |  DISEASES
9960  |  USP3  |  DISEASES
148  |  ADRA1A  |  DISEASES
2788  |  GNG7  |  DISEASES
116448  |  OLIG1  |  DISEASES
1814  |  DRD3  |  DISEASES
83696  |  TRAPPC9  |  DISEASES
22900  |  CARD8  |  DISEASES
1621  |  DBH  |  DISEASES
8301  |  PICALM  |  DISEASES
26468  |  LHX6  |  DISEASES
2643  |  GCH1  |  DISEASES
64221  |  ROBO3  |  DISEASES
55112  |  WDR60  |  DISEASES
9378  |  NRXN1  |  DISEASES
152  |  ADRA2C  |  DISEASES
1363  |  CPE  |  DISEASES
114781  |  BTBD9  |  DISEASES
93986  |  FOXP2  |  DISEASES
57282  |  SLC4A10  |  DISEASES
4204  |  MECP2  |  DISEASES
8910  |  SGCE  |  DISEASES
136306  |  SVOPL  |  DISEASES
2195  |  FAT1  |  DISEASES
1408  |  CRY2  |  DISEASES
1139  |  CHRNA7  |  DISEASES
2668  |  GDNF  |  DISEASES
627  |  BDNF  |  DISEASES
79012  |  CAMKV  |  DISEASES
266553  |  OFCC1  |  DISEASES
221823  |  PRPS1L1  |  DISEASES
23286  |  WWC1  |  DISEASES
6586  |  SLIT3  |  DISEASES
3748  |  KCNC3  |  DISEASES
64478  |  CSMD1  |  DISEASES
6999  |  TDO2  |  DISEASES
80184  |  CEP290  |  DISEASES
321  |  APBA2  |  DISEASES
820  |  CAMP  |  DISEASES
102723508  |  KANTR  |  DISEASES
359809  |  PEG13  |  DISEASES
Locus(Waiting for update.)
Disease ID 854
Disease tic disorder
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:213)
HP:0000737  |  Irritability  |  22
HP:0001249  |  Mental retardation  |  21
HP:0100753  |  Schizophrenia  |  20
HP:0100543  |  Cognitive deficits  |  18
HP:0001631  |  Atria septal defect  |  17
HP:0000717  |  Autism  |  8
HP:0000708  |  Behavioral problems  |  7
HP:0000716  |  Depression  |  7
HP:0000739  |  Anxiety  |  7
HP:0003774  |  End-stage renal failure  |  6
HP:0001250  |  Seizures  |  6
HP:0000738  |  Sensory hallucination  |  6
HP:0000746  |  Delusions  |  6
HP:0000709  |  Psychosis  |  6
HP:0001903  |  Anemia  |  6
HP:0002960  |  Autoimmune condition  |  6
HP:0007302  |  Bipolar disorder  |  6
HP:0000822  |  Hypertension  |  5
HP:0000726  |  Dementia  |  5
HP:0000718  |  Aggressive behaviour  |  5
HP:0000083  |  Renal insufficiency  |  5
HP:0000722  |  Obsessive compulsive disorder  |  5
HP:0001513  |  Obesity  |  5
HP:0000365  |  Hearing impairment  |  5
HP:0100033  |  Tic disorder  |  4
HP:0003287  |  Abnormality of mitochondrial metabolism  |  4
HP:0005528  |  Bone marrow hypoplasia  |  4
HP:0001394  |  Hepatic cirrhosis  |  4
HP:0001873  |  Low platelet count  |  4
HP:0000078  |  Genital abnormalities  |  3
HP:0004322  |  Stature below 3rd percentile  |  3
HP:0100785  |  Insomnia  |  3
HP:0011675  |  Arrhythmias  |  3
HP:0002092  |  Pulmonary artery hypertension  |  3
HP:0000787  |  Renal calculi  |  3
HP:0001067  |  Neurofibromas  |  3
HP:0001627  |  Congenital heart defects  |  3
HP:0002758  |  Osteoarthritis  |  3
HP:0004308  |  Ventricular arrhythmia  |  3
HP:0003128  |  Lactic acidosis  |  3
HP:0012622  |  Chronic kidney disease  |  2
HP:0012115  |  Liver inflammation  |  2
HP:0000704  |  Pyorrhea  |  2
HP:0008765  |  Auditory hallucinations  |  2
HP:0002902  |  Hyponatremia  |  2
HP:0002621  |  Atherosclerosis  |  2
HP:0008258  |  Congenital adrenal hyperplasia  |  2
HP:0001677  |  Coronary artery disease  |  2
HP:0001257  |  Spasticity  |  2
HP:0000113  |  Polycystic kidney dysplasia  |  2
HP:0002353  |  Abnormal EEG  |  2
HP:0000833  |  Glucose intolerance  |  2
HP:0100614  |  Muscle inflammation  |  2
HP:0008221  |  Enlarged adrenal glands  |  2
HP:0100710  |  Impulsivity  |  2
HP:0002721  |  Immunodeficiency  |  2
HP:0002315  |  Headaches  |  2
HP:0002665  |  Lymphoma  |  2
HP:0100522  |  Thymoma  |  2
HP:0001258  |  Spastic paraplegia, lower limb  |  2
HP:0010550  |  Paraplegia  |  2
HP:0005181  |  Premature coronary artery disease  |  2
HP:0012532  |  Chronic pain  |  2
HP:0000729  |  Pervasive developmental disorder  |  2
HP:0001397  |  Hepatic steatosis  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0001510  |  Growth deficiency  |  2
HP:0000501  |  Glaucoma  |  2
HP:0012531  |  Pain  |  2
HP:0000563  |  Conical cornea  |  2
HP:0007018  |  Attention deficits  |  2
HP:0000752  |  Hyperactive behavior  |  2
HP:0002639  |  Budd-Chiari syndrome  |  2
HP:0000027  |  Azoospermia  |  1
HP:0012490  |  Inflammation of fat tissue  |  1
HP:0000093  |  Proteinuria  |  1
HP:0006510  |  Chronic obstructive pulmonary disease  |  1
HP:0001268  |  Mental deterioration  |  1
HP:0011096  |  Demyelination  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0002459  |  Dysautonomia  |  1
HP:0000924  |  Abnormality of the skeletal system  |  1
HP:0002071  |  Extrapyramidal dysfunction  |  1
HP:0012758  |  Neurodevelopmental delay  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0001087  |  Childhood glaucoma  |  1
HP:0009589  |  Bilateral vestibular Schwannoma  |  1
HP:0005206  |  Pancreatic pseudocyst  |  1
HP:0009588  |  Vestibular Schwannoma  |  1
HP:0006706  |  Cystic liver disease  |  1
HP:0000657  |  Oculomotor apraxia  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0002953  |  Vertebral compression fractures  |  1
HP:0002186  |  Apraxia  |  1
HP:0003690  |  Limb weakness  |  1
HP:0011999  |  Paranoia  |  1
HP:0001943  |  Hypoglycemia  |  1
HP:0003323  |  Muscle weakness, progressive  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0100660  |  Dyskinesis  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0001324  |  Muscular weakness  |  1
HP:0100774  |  Hyperostosis  |  1
HP:0000750  |  Late-onset speech development  |  1
HP:0002608  |  Celiac disease  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0002073  |  Cerebellar ataxia, progressive  |  1
HP:0000989  |  pruritis  |  1
HP:0100962  |  Shyness  |  1
HP:0009732  |  Plexiform neurofibroma  |  1
HP:0000107  |  Renal cyst  |  1
HP:0001650  |  Valvular aortic stenosis  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0000998  |  Hypertrichosis  |  1
HP:0002283  |  Global brain atrophy  |  1
HP:0002958  |  Immune dysregulation  |  1
HP:0000618  |  Blindness  |  1
HP:0040075  |  Hypopituitarism  |  1
HP:0001396  |  Cholestasis  |  1
HP:0002591  |  Voracious appetite  |  1
HP:0000853  |  Goitre  |  1
HP:0003231  |  Increased tyrosine in blood  |  1
HP:0001300  |  Parkinsonism  |  1
HP:0003072  |  Hypercalcemia  |  1
HP:0006557  |  Polycystic liver disease  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0002313  |  Spastic paraparesis  |  1
HP:0012743  |  Central obesity  |  1
HP:0011947  |  Respiratory infection  |  1
HP:0000757  |  Lack of insight  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0001978  |  Extramedullary hematopoiesis  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0009826  |  limb shortening  |  1
HP:0003418  |  Back pain  |  1
HP:0004554  |  Generalized hypertrichosis  |  1
HP:0000510  |  Retinitis pigmentosa  |  1
HP:0004349  |  Reduced bone mineral density  |  1
HP:0000256  |  Macrocrania  |  1
HP:0002360  |  Sleep disturbance  |  1
HP:0000252  |  Small head circumference  |  1
HP:0002342  |  Intellectual disability, moderate  |  1
HP:0002385  |  Paraparesis  |  1
HP:0100034  |  Motor tics  |  1
HP:0001824  |  Weight loss  |  1
HP:0012075  |  Personality disorder  |  1
HP:0012444  |  Brain wasting  |  1
HP:0003510  |  Proportionate dwarfism  |  1
HP:0000713  |  Agitation  |  1
HP:0100324  |  Progressive systemic scleroderma  |  1
HP:0000556  |  Retinal dystrophy  |  1
HP:0002664  |  Neoplasia  |  1
HP:0001263  |  Developmental retardation  |  1
HP:0000825  |  Hyperinsulinaemic hypoglycaemia  |  1
HP:0200044  |  Porokeratosis  |  1
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  1
HP:0000166  |  Severe periodontal disease  |  1
HP:0002155  |  Increased triglycerides  |  1
HP:0002650  |  Scoliosis  |  1
HP:0001935  |  Microcytic anemia  |  1
HP:0000010  |  Frequent urinary tract infections  |  1
HP:0000028  |  Cryptorchidism  |  1
HP:0004493  |  Hyperostosis of craniofacial bones  |  1
HP:0012226  |  Ovarian teratoma  |  1
HP:0000024  |  Inflammation of the prostate  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0012378  |  Fatigue  |  1
HP:0001875  |  Neutropenia  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0100022  |  Movement disorder  |  1
HP:0001363  |  Early fusion of cranial sutures  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0002573  |  Bloody diarrhea  |  1
HP:0009775  |  Amniotic constriction ring  |  1
HP:0002901  |  Hypocalcemia  |  1
HP:0001643  |  Persistent ductus arteriosus  |  1
HP:0001733  |  Pancreatic inflammation  |  1
HP:0002625  |  Blood clot in a deep vein  |  1
HP:0000020  |  Bladder incontinence  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0000789  |  Infertility  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0007199  |  Progressive spastic paraparesis  |  1
HP:0002659  |  Increased tendency to fractures  |  1
HP:0002633  |  Vasculitis  |  1
HP:0001562  |  Oligohydramnios  |  1
HP:0003537  |  Low blood uric acid levels  |  1
HP:0005484  |  Acquired microcephaly  |  1
HP:0100806  |  Sepsis  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0001548  |  Overgrowth  |  1
HP:0000505  |  Poor vision  |  1
HP:0040012  |  Tendency to chromosomal breakage  |  1
HP:0000546  |  Retinal degeneration  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0010310  |  Chylothorax  |  1
HP:0001332  |  Dystonia  |  1
HP:0001369  |  Arthritis  |  1
HP:0002072  |  Chorea  |  1
HP:0001009  |  Telangiectases  |  1
HP:0003124  |  Elevated serum cholesterol  |  1
HP:0001251  |  Ataxia  |  1
HP:0030083  |  Salt craving  |  1
HP:0000992  |  Skin photosensitivity  |  1
HP:0004381  |  Supravalvular aortic stenosis  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0005086  |  Knee osteoarthritis  |  1
Disease ID 854
Disease tic disorder
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs6311172418283356HTR2Aumls:C0040188BeFreeNominally 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.0.0005428842007HTR2A1346897343CT
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
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.)
Chemical(Total Drugs:21)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0040188aripiprazoleD000068180-tic disordersMESH:D013981therapeutic15358981
C0040188caffeineD0021101958/8/2tic disordersMESH:D013981marker/mechanism9606246
C0040188carbamazepineD002220298-46-4tic disordersMESH:D013981marker/mechanism10937170
C0040188citalopramD01528359729-33-8tic disordersMESH:D013981marker/mechanism15812270
C0040188clonidineD0030004205-90-7tic disordersMESH:D013981marker/mechanism11392527
C0040188clozapineD0030245786-21-0tic disordersMESH:D013981marker/mechanism15701074
C0040188fluoxetineD00547354910-89-3tic disordersMESH:D013981marker/mechanism2356881
C0040188fluvoxamineD01666654739-18-3tic disordersMESH:D013981marker/mechanism10434483
C0040188haloperidolD00622052-86-8tic disordersMESH:D013981marker/mechanism1536082
C0040188haloperidolD00622052-86-8tic disordersMESH:D013981therapeutic15358981
C0040188methylphenidateD008774113-45-1tic disordersMESH:D013981marker/mechanism1061848
C0040188methylphenidateD008774113-45-1tic disordersMESH:D013981therapeutic7560119
C0040188ofloxacinD01524282419-36-1tic disordersMESH:D013981marker/mechanism8835045
C0040188pramipexoleC061333-tic disordersMESH:D013981marker/mechanism18181204
C0040188valproic acidD01463599-66-1tic disordersMESH:D013981therapeutic15701074
C0040188fluoxetineD00547354910-89-3ticsMESH:D020323therapeutic2057015
C0040188haloperidolD00622052-86-8ticsMESH:D020323therapeutic269683
C0040188methylphenidateD008774113-45-1ticsMESH:D020323marker/mechanism2016228
C0040188nicotineD009538-ticsMESH:D020323therapeutic15774505
C0040188nortriptylineD00966172-69-5ticsMESH:D020323marker/mechanism2708560
C0040188oxycodoneD01009876-42-6ticsMESH:D020323therapeutic2057015
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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