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Pediatric Disease Annotations & Medicines



   hyperthyroidism
  

Disease ID 320
Disease hyperthyroidism
Definition
Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE.
Synonym
hyperthyroid
hyperthyroidism (disorder)
hyperthyroidism [disease/finding]
hyperthyroidism nos
hyperthyroidism, nos
hyperthyroids
overactive thyroid
DOID
UMLS
C0020550
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:160)
C0018213  |  graves' disease  |  21
C0018021  |  goiter  |  14
C0020676  |  hypothyroidism  |  13
C0018799  |  heart disease  |  12
C0018801  |  heart failure  |  12
C0010068  |  coronary heart disease  |  9
C0020538  |  hypertension  |  9
C0040147  |  thyroiditis  |  9
C0007115  |  thyroid ca  |  7
C0011847  |  diabetes  |  6
C0040156  |  thyrotoxicosis  |  6
C0040137  |  thyroid nodule  |  6
C0007115  |  thyroid cancer  |  5
C0029456  |  osteoporosis  |  5
C0018021  |  goitre  |  5
C0027051  |  myocardial infarction  |  4
C0018023  |  nodular goiter  |  4
C0030312  |  pancytopenia  |  4
C0027051  |  myocardial infarct  |  4
C0018802  |  congestive heart failure  |  4
C0001430  |  adenoma  |  4
C0878544  |  cardiomyopathy  |  4
C0151468  |  thyroid adenoma  |  4
C0040053  |  thrombosis  |  3
C0020676  |  hypothyroid  |  3
C0032000  |  pituitary adenoma  |  3
C0398623  |  hypercoagulable state  |  3
C0018801  |  cardiac failure  |  3
C0030443  |  periodic paralysis  |  3
C0020450  |  hyperemesis gravidarum  |  3
C0020542  |  pulmonary hypertension  |  3
C0398623  |  hypercoagulability  |  3
C0238358  |  hypokalemic periodic paralysis  |  3
C0235250  |  hyperemesis  |  3
C0022661  |  chronic kidney disease  |  2
C0004096  |  asthma  |  2
C0010278  |  craniosynostosis  |  2
C0022116  |  ischemia  |  2
C0042373  |  vascular disorder  |  2
C0497327  |  dementia  |  2
C0026848  |  muscular disorders  |  2
C0155626  |  acute myocardial infarction  |  2
C0020550  |  hyperthyroidism  |  2
C0042373  |  vascular disorders  |  2
C0342199  |  iodine deficiency  |  2
C0040137  |  thyroid nodules  |  2
C0030319  |  panic disorder  |  2
C0042870  |  vitamin d deficiency  |  2
C0001824  |  agranulocytosis  |  2
C0342208  |  multinodular goitre  |  2
C0677607  |  hashimoto thyroiditis  |  2
C0018213  |  graves disease  |  2
C0745140  |  hyperthyroid  |  2
C0026848  |  myopathy  |  2
C0040128  |  thyroid disease  |  2
C0007222  |  cardiovascular disorders  |  2
C0040127  |  thyroid storm  |  2
C0018023  |  nodular goitre  |  2
C0020437  |  hypercalcemia  |  2
C0032914  |  preeclampsia  |  2
C0023895  |  liver disease  |  2
C0011570  |  depression  |  2
C0034065  |  pulmonary embolism  |  2
C0002871  |  anemia  |  2
C0042870  |  vitamin d defic  |  2
C0033975  |  psychosis  |  2
C0549473  |  thyroid carcinoma  |  2
C0023418  |  leukemia  |  1
C0033038  |  premature ejaculation  |  1
C0000809  |  recurrent miscarriage  |  1
C0011848  |  diabetes insipidus  |  1
C0677607  |  hashimoto's disease  |  1
C0206682  |  follicular carcinoma  |  1
C0002170  |  alopecia  |  1
C1619734  |  pulmonary arterial hypertension  |  1
C0018024  |  retrosternal goitre  |  1
C0019196  |  hepatitis c  |  1
C0022661  |  end stage renal disease (esrd)  |  1
C0002395  |  alzheimer's disease  |  1
C0015397  |  eye disease  |  1
C0027145  |  myxedema  |  1
C0000809  |  recurrent miscarriages  |  1
C0018799  |  heart diseases  |  1
C0025183  |  meige's syndrome  |  1
C0010308  |  cretinism  |  1
C0019158  |  hepatitis  |  1
C0032000  |  pituitary adenomas  |  1
C0000786  |  miscarriage  |  1
C0008370  |  cholestasis  |  1
C0034372  |  quadriplegia  |  1
C0040100  |  thymoma  |  1
C0018024  |  intrathoracic goiter  |  1
C0152025  |  polyneuropathy  |  1
C0041696  |  major depressive disorder  |  1
C0004153  |  atherosclerosis  |  1
C0028754  |  obesity  |  1
C0042384  |  vasculitis  |  1
C0020456  |  hyperglycemia  |  1
C0159069  |  impaired glucose tolerance  |  1
C0002878  |  hemolytic anemia  |  1
C0022658  |  renal disease  |  1
C0042164  |  uveitis  |  1
C0009171  |  cocaine abuse  |  1
C0026896  |  myasthenia gravis  |  1
C0040150  |  acute suppurative thyroiditis  |  1
C0238463  |  papillary thyroid carcinoma  |  1
C0022354  |  cholestatic jaundice  |  1
C0042900  |  vitiligo  |  1
C0022658  |  nephropathy  |  1
C1135868  |  gestational trophoblastic neoplasia  |  1
C0272126  |  evans' syndrome  |  1
C0242520  |  chronic thyroiditis  |  1
C0031039  |  pericardial effusion  |  1
C0021053  |  immune disease  |  1
C0085681  |  hyperphosphatemia  |  1
C0013395  |  indigestion  |  1
C0013473  |  eating disorders  |  1
C0339143  |  thyroid ophthalmopathy  |  1
C0010481  |  cushing syndrome  |  1
C0022658  |  kidney disease  |  1
C0004096  |  bronchial asthma  |  1
C0006142  |  breast cancer  |  1
C0011860  |  type 2 diabetes  |  1
C0013384  |  dyskinesia  |  1
C0242231  |  coronary stenoses  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C1140680  |  malignant ovarian tumor  |  1
C1868720  |  periventricular nodular heterotopia  |  1
C0018799  |  cardiac disease  |  1
C0004245  |  atrioventricular block  |  1
C0262587  |  parathyroid adenoma  |  1
C0032002  |  pituitary disease  |  1
C0002871  |  anaemia  |  1
C0022116  |  ischaemia  |  1
C0030920  |  peptic ulcer  |  1
C0031511  |  pheochromocytoma  |  1
C0152171  |  idiopathic pulmonary hypertension  |  1
C0151740  |  increased intracranial pressure  |  1
C0342208  |  multinodular goiter  |  1
C0030499  |  parasitosis  |  1
C0020502  |  hyperparathyroidism  |  1
C0018099  |  gout  |  1
C0221002  |  primary hyperparathyroidism  |  1
C0030567  |  parkinson's disease  |  1
C0339143  |  thyroid eye disease  |  1
C0920350  |  autoimmune thyroiditis  |  1
C0259779  |  fibrous dysplasia  |  1
C0010073  |  coronary spasm  |  1
C0033687  |  proteinuria  |  1
C0013473  |  eating disorder  |  1
C0027868  |  neuromuscular disorders  |  1
C0339143  |  graves' ophthalmopathy  |  1
C0242604  |  thyroid hormone resistance  |  1
C0154143  |  toxic multinodular goitre  |  1
C0085655  |  polymyositis  |  1
C0034013  |  precocious puberty  |  1
C0005586  |  bipolar disorder  |  1
C0042721  |  viral hepatitis  |  1
C0022661  |  end stage renal disease  |  1
C0677607  |  hashimoto's thyroiditis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:9)
SOD1  |  6647  |  CTD_human
SOD2  |  6648  |  CTD_human
PON1  |  5444  |  CTD_human
AQP1  |  358  |  CTD_human
TSHR  |  7253  |  CTD_human
GPX1  |  2876  |  CTD_human
CAT  |  847  |  CTD_human
CARTPT  |  9607  |  CTD_human
GSR  |  2936  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
4524  |  MTHFR  |  infer
7421  |  VDR  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:325)
6515  |  SLC2A3  |  DISEASES
1361  |  CPB2  |  DISEASES
27102  |  EIF2AK1  |  DISEASES
9552  |  SPAG7  |  DISEASES
4320  |  MMP11  |  DISEASES
84844  |  PHF5A  |  DISEASES
5020  |  OXT  |  DISEASES
23439  |  ATP1B4  |  DISEASES
54  |  ACP5  |  DISEASES
7038  |  TG  |  DISEASES
1666  |  DECR1  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
56729  |  RETN  |  DISEASES
973  |  CD79A  |  DISEASES
9545  |  RAB3D  |  DISEASES
6528  |  SLC5A5  |  DISEASES
5054  |  SERPINE1  |  DISEASES
4353  |  MPO  |  DISEASES
5691  |  PSMB3  |  DISEASES
80157  |  CWH43  |  DISEASES
3558  |  IL2  |  DISEASES
4256  |  MGP  |  DISEASES
3458  |  IFNG  |  DISEASES
389434  |  IYD  |  DISEASES
6908  |  TBP  |  DISEASES
2690  |  GHR  |  DISEASES
3565  |  IL4  |  DISEASES
338  |  APOB  |  DISEASES
3488  |  IGFBP5  |  DISEASES
566  |  AZU1  |  DISEASES
4953  |  ODC1  |  DISEASES
5657  |  PRTN3  |  DISEASES
335  |  APOA1  |  DISEASES
7276  |  TTR  |  DISEASES
134637  |  ADAT2  |  DISEASES
2691  |  GHRH  |  DISEASES
8074  |  FGF23  |  DISEASES
57616  |  TSHZ3  |  DISEASES
2693  |  GHSR  |  DISEASES
4852  |  NPY  |  DISEASES
3759  |  KCNJ2  |  DISEASES
7355  |  SLC35A2  |  DISEASES
4974  |  OMG  |  DISEASES
2678  |  GGT1  |  DISEASES
11135  |  CDC42EP1  |  DISEASES
482  |  ATP1B2  |  DISEASES
3630  |  INS  |  DISEASES
3741  |  KCNA5  |  DISEASES
27112  |  FAM155B  |  DISEASES
376497  |  SLC27A1  |  DISEASES
2056  |  EPO  |  DISEASES
50617  |  ATP6V0A4  |  DISEASES
23378  |  RRP8  |  DISEASES
1401  |  CRP  |  DISEASES
4922  |  NTS  |  DISEASES
759  |  CA1  |  DISEASES
7252  |  TSHB  |  DISEASES
2694  |  GIF  |  DISEASES
79074  |  C2orf49  |  DISEASES
3569  |  IL6  |  DISEASES
29113  |  C6orf15  |  DISEASES
51163  |  DBR1  |  DISEASES
29953  |  TRHDE  |  DISEASES
7450  |  VWF  |  DISEASES
54947  |  LPCAT2  |  DISEASES
4591  |  TRIM37  |  DISEASES
28965  |  SLC27A6  |  DISEASES
5465  |  PPARA  |  DISEASES
671  |  BPI  |  DISEASES
25939  |  SAMHD1  |  DISEASES
7350  |  UCP1  |  DISEASES
3553  |  IL1B  |  DISEASES
27143  |  PALD1  |  DISEASES
1991  |  ELANE  |  DISEASES
56981  |  PRDM11  |  DISEASES
832  |  CAPZB  |  DISEASES
84273  |  NOA1  |  DISEASES
79031  |  PDCL3  |  DISEASES
7067  |  THRA  |  DISEASES
5443  |  POMC  |  DISEASES
3383  |  ICAM1  |  DISEASES
1950  |  EGF  |  DISEASES
5172  |  SLC26A4  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
3705  |  ITPK1  |  DISEASES
3480  |  IGF1R  |  DISEASES
55520  |  ELAC1  |  DISEASES
3487  |  IGFBP4  |  DISEASES
126374  |  WTIP  |  DISEASES
5226  |  PGD  |  DISEASES
5972  |  REN  |  DISEASES
23549  |  DNPEP  |  DISEASES
185  |  AGTR1  |  DISEASES
3484  |  IGFBP1  |  DISEASES
6567  |  SLC16A2  |  DISEASES
84636  |  GPR174  |  DISEASES
2796  |  GNRH1  |  DISEASES
1392  |  CRH  |  DISEASES
3439  |  IFNA1  |  DISEASES
3606  |  IL18  |  DISEASES
7069  |  THRSP  |  DISEASES
23704  |  KCNE4  |  DISEASES
5163  |  PDK1  |  DISEASES
5741  |  PTH  |  DISEASES
1420  |  CRYGC  |  DISEASES
339896  |  GADL1  |  DISEASES
23250  |  ATP11A  |  DISEASES
4900  |  NRGN  |  DISEASES
6750  |  SST  |  DISEASES
222696  |  ZSCAN23  |  DISEASES
56683  |  C21orf59  |  DISEASES
539  |  ATP5O  |  DISEASES
1636  |  ACE  |  DISEASES
181  |  AGRP  |  DISEASES
3101  |  HK3  |  DISEASES
6755  |  SSTR5  |  DISEASES
7412  |  VCAM1  |  DISEASES
3973  |  LHCGR  |  DISEASES
4880  |  NPPC  |  DISEASES
213  |  ALB  |  DISEASES
117156  |  SCGB3A2  |  DISEASES
9607  |  CARTPT  |  DISEASES
94120  |  SYTL3  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
7253  |  TSHR  |  DISEASES
11067  |  C10orf10  |  DISEASES
27343  |  POLL  |  DISEASES
6447  |  SCG5  |  DISEASES
3904  |  LAIR2  |  DISEASES
956  |  ENTPD3  |  DISEASES
5617  |  PRL  |  DISEASES
3479  |  IGF1  |  DISEASES
7200  |  TRH  |  DISEASES
1493  |  CTLA4  |  DISEASES
219409  |  GSX1  |  DISEASES
260425  |  MAGI3  |  DISEASES
84342  |  COG8  |  DISEASES
5066  |  PAM  |  DISEASES
2353  |  FOS  |  DISEASES
147  |  ADRA1B  |  DISEASES
4632  |  MYL1  |  DISEASES
4176  |  MCM7  |  DISEASES
5122  |  PCSK1  |  DISEASES
2147  |  F2  |  DISEASES
3626  |  INHBC  |  DISEASES
5340  |  PLG  |  DISEASES
10008  |  KCNE3  |  DISEASES
7351  |  UCP2  |  DISEASES
3952  |  LEP  |  DISEASES
55584  |  CHRNA9  |  DISEASES
2688  |  GH1  |  DISEASES
81832  |  NETO1  |  DISEASES
3737  |  KCNA2  |  DISEASES
201164  |  PLD6  |  DISEASES
22864  |  R3HDM2  |  DISEASES
7173  |  TPO  |  DISEASES
132243  |  H1FOO  |  DISEASES
23428  |  SLC7A8  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
64787  |  EPS8L2  |  DISEASES
6517  |  SLC2A4  |  DISEASES
6863  |  TAC1  |  DISEASES
4018  |  LPA  |  DISEASES
4808  |  NHLH2  |  DISEASES
2274  |  FHL2  |  DISEASES
7352  |  UCP3  |  DISEASES
91012  |  CERS5  |  DISEASES
2187  |  FANCB  |  DISEASES
2863  |  GPR39  |  DISEASES
3768  |  KCNJ12  |  DISEASES
114786  |  XKR4  |  DISEASES
3739  |  KCNA4  |  DISEASES
6906  |  SERPINA7  |  DISEASES
29110  |  TBK1  |  DISEASES
283869  |  NPW  |  DISEASES
2831  |  NPBWR1  |  DISEASES
2520  |  GAST  |  DISEASES
3772  |  KCNJ15  |  DISEASES
6401  |  SELE  |  DISEASES
796  |  CALCA  |  DISEASES
3751  |  KCND2  |  DISEASES
353164  |  TAS2R42  |  DISEASES
2152  |  F3  |  DISEASES
5133  |  PDCD1  |  DISEASES
51738  |  GHRL  |  DISEASES
93974  |  ATPIF1  |  DISEASES
135  |  ADORA2A  |  DISEASES
1103  |  CHAT  |  DISEASES
3363  |  HTR7  |  DISEASES
23583  |  SMUG1  |  DISEASES
114904  |  C1QTNF6  |  DISEASES
84144  |  SYDE2  |  DISEASES
3770  |  KCNJ14  |  DISEASES
10488  |  CREB3  |  DISEASES
866  |  SERPINA6  |  DISEASES
31  |  ACACA  |  DISEASES
7316  |  UBC  |  DISEASES
2624  |  GATA2  |  DISEASES
100132406  |  NBPF10  |  DISEASES
3767  |  KCNJ11  |  DISEASES
51322  |  WAC  |  DISEASES
286133  |  SCARA5  |  DISEASES
4624  |  MYH6  |  DISEASES
7068  |  THRB  |  DISEASES
487  |  ATP2A1  |  DISEASES
6752  |  SSTR2  |  DISEASES
2764  |  GMFB  |  DISEASES
10004  |  NAALADL1  |  DISEASES
1735  |  DIO3  |  DISEASES
9464  |  HAND2  |  DISEASES
57181  |  SLC39A10  |  DISEASES
26191  |  PTPN22  |  DISEASES
4151  |  MB  |  DISEASES
51150  |  SDF4  |  DISEASES
2157  |  F8  |  DISEASES
80274  |  SCUBE1  |  DISEASES
23245  |  ASTN2  |  DISEASES
1733  |  DIO1  |  DISEASES
10724  |  MGEA5  |  DISEASES
779  |  CACNA1S  |  DISEASES
54617  |  INO80  |  DISEASES
23038  |  WDTC1  |  DISEASES
183  |  AGT  |  DISEASES
22796  |  COG2  |  DISEASES
11116  |  FGFR1OP  |  DISEASES
6993  |  DYNLT1  |  DISEASES
7432  |  VIP  |  DISEASES
481  |  ATP1B1  |  DISEASES
55811  |  ADCY10  |  DISEASES
336  |  APOA2  |  DISEASES
844  |  CASQ1  |  DISEASES
115352  |  FCRL3  |  DISEASES
632  |  BGLAP  |  DISEASES
64077  |  LHPP  |  DISEASES
117247  |  SLC16A10  |  DISEASES
262  |  AMD1  |  DISEASES
153  |  ADRB1  |  DISEASES
4803  |  NGF  |  DISEASES
2832  |  NPBWR2  |  DISEASES
959  |  CD40LG  |  DISEASES
2778  |  GNAS  |  DISEASES
26027  |  ACOT11  |  DISEASES
3745  |  KCNB1  |  DISEASES
8022  |  LHX3  |  DISEASES
958  |  CD40  |  DISEASES
90550  |  MCU  |  DISEASES
9452  |  ITM2A  |  DISEASES
252995  |  FNDC5  |  DISEASES
253430  |  IPMK  |  DISEASES
1043  |  CD52  |  DISEASES
23732  |  FRRS1L  |  DISEASES
6257  |  RXRB  |  DISEASES
2304  |  FOXE1  |  DISEASES
3055  |  HCK  |  DISEASES
50943  |  FOXP3  |  DISEASES
4879  |  NPPB  |  DISEASES
4878  |  NPPA  |  DISEASES
6992  |  PPP1R11  |  DISEASES
3105  |  HLA-A  |  DISEASES
1471  |  CST3  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
57380  |  MRS2  |  DISEASES
2782  |  GNB1  |  DISEASES
1906  |  EDN1  |  DISEASES
5160  |  PDHA1  |  DISEASES
3440  |  IFNA2  |  DISEASES
3456  |  IFNB1  |  DISEASES
551  |  AVP  |  DISEASES
6462  |  SHBG  |  DISEASES
3486  |  IGFBP3  |  DISEASES
5618  |  PRLR  |  DISEASES
6649  |  SOD3  |  DISEASES
83650  |  SLC35G5  |  DISEASES
54476  |  RNF216  |  DISEASES
6996  |  TDG  |  DISEASES
6152  |  RPL24  |  DISEASES
4828  |  NMB  |  DISEASES
79001  |  VKORC1  |  DISEASES
56624  |  ASAH2  |  DISEASES
816  |  CAMK2B  |  DISEASES
5744  |  PTHLH  |  DISEASES
144195  |  SLC2A14  |  DISEASES
55234  |  SMU1  |  DISEASES
594857  |  NPS  |  DISEASES
6345  |  SRL  |  DISEASES
10587  |  TXNRD2  |  DISEASES
2492  |  FSHR  |  DISEASES
3098  |  HK1  |  DISEASES
728441  |  GGT2  |  DISEASES
7018  |  TF  |  DISEASES
10989  |  IMMT  |  DISEASES
3267  |  AGFG1  |  DISEASES
2641  |  GCG  |  DISEASES
5073  |  PARN  |  DISEASES
8604  |  SLC25A12  |  DISEASES
4295  |  MLN  |  DISEASES
3481  |  IGF2  |  DISEASES
201456  |  FBXO15  |  DISEASES
7849  |  PAX8  |  DISEASES
6329  |  SCN4A  |  DISEASES
7124  |  TNF  |  DISEASES
51562  |  MBIP  |  DISEASES
84290  |  CAPNS2  |  DISEASES
2145  |  EZH1  |  DISEASES
3451  |  IFNA17  |  DISEASES
6513  |  SLC2A1  |  DISEASES
4700  |  NDUFA6  |  DISEASES
2317  |  FLNB  |  DISEASES
5164  |  PDK2  |  DISEASES
51428  |  DDX41  |  DISEASES
8635  |  RNASET2  |  DISEASES
4975  |  OMP  |  DISEASES
930  |  CD19  |  DISEASES
100288485  |  MTRNR2L7  |  DISEASES
488  |  ATP2A2  |  DISEASES
3250  |  HPR  |  DISEASES
6999  |  TDO2  |  DISEASES
4850  |  CNOT4  |  DISEASES
1734  |  DIO2  |  DISEASES
567  |  B2M  |  DISEASES
5297  |  PI4KA  |  DISEASES
102723508  |  KANTR  |  DISEASES
348120  |  LINC01193  |  DISEASES
23642  |  SNHG1  |  DISEASES
27004  |  TCL6  |  DISEASES
Locus(Waiting for update.)
Disease ID 320
Disease hyperthyroidism
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:143)
HP:0000853  |  Goitre  |  19
HP:0005110  |  Atrial fibrillation  |  18
HP:0000821  |  Underactive thyroid  |  13
HP:0001635  |  Congestive heart failure  |  13
HP:0100646  |  Thyroiditis  |  9
HP:0000822  |  Hypertension  |  9
HP:0000855  |  Insulin resistance  |  8
HP:0001824  |  Weight loss  |  6
HP:0000939  |  Osteoporosis  |  5
HP:0002900  |  Hypokalemia  |  4
HP:0011675  |  Arrhythmias  |  4
HP:0001638  |  Cardiomyopathy  |  4
HP:0000854  |  Thyroid adenoma  |  4
HP:0005994  |  Nodular goiter  |  4
HP:0001876  |  Low blood cell count  |  4
HP:0002092  |  Pulmonary artery hypertension  |  4
HP:0012188  |  Hyperemesis gravidarum  |  3
HP:0002893  |  Pituitary adenoma  |  3
HP:0001903  |  Anemia  |  3
HP:0003768  |  Periodic paralysis  |  3
HP:0000872  |  Hashimoto's thyroiditis  |  3
HP:0003470  |  Inability to move  |  3
HP:0000836  |  Overactive thyroid  |  3
HP:0001658  |  Myocardial infarction  |  3
HP:0030731  |  Carcinoma  |  3
HP:0001297  |  Cerebral vascular events  |  3
HP:0000952  |  Yellow skin  |  3
HP:0100724  |  Hypercoagulability  |  3
HP:0001649  |  Tachycardia  |  3
HP:0003198  |  Myopathic changes  |  2
HP:0100602  |  Pre-eclampsia  |  2
HP:0001324  |  Muscular weakness  |  2
HP:0000938  |  Decreased bone mineral density  |  2
HP:0000709  |  Psychosis  |  2
HP:0011665  |  Takotsubo cardiomyopathy  |  2
HP:0002925  |  Increased serum thyroid-stimulating hormone  |  2
HP:0001907  |  Thromboembolic disease  |  2
HP:0000820  |  Thyroid abnormality  |  2
HP:0002072  |  Chorea  |  2
HP:0002664  |  Neoplasia  |  2
HP:0002015  |  Swallowing difficulty  |  2
HP:0001363  |  Early fusion of cranial sutures  |  2
HP:0002099  |  Asthma  |  2
HP:0003072  |  Hypercalcemia  |  2
HP:0000752  |  Hyperactive behavior  |  2
HP:0100647  |  Morbus Basedow  |  2
HP:0000969  |  Dropsy  |  2
HP:0100512  |  Vitamin D deficiency  |  2
HP:0002204  |  Pulmonary embolism  |  2
HP:0012234  |  Agranulocytosis  |  2
HP:0002930  |  Resistance to thyroid hormone  |  2
HP:0002890  |  Thyroid carcinoma  |  2
HP:0001511  |  Prenatal onset growth retardation  |  2
HP:0000726  |  Dementia  |  2
HP:0100029  |  Lingual thyroid  |  2
HP:0012622  |  Chronic kidney disease  |  2
HP:0001399  |  Liver failure  |  2
HP:0003287  |  Abnormality of mitochondrial metabolism  |  2
HP:0000716  |  Depression  |  2
HP:0002046  |  Heat intolerance  |  2
HP:0004349  |  Reduced bone mineral density  |  2
HP:0004936  |  Blood clot in vein  |  2
HP:0002591  |  Voracious appetite  |  1
HP:0004308  |  Ventricular arrhythmia  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0001396  |  Cholestasis  |  1
HP:0001250  |  Seizures  |  1
HP:0002150  |  Hypercalcinuria  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0001623  |  Breech presentation at birth  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0001622  |  Premature delivery  |  1
HP:0012876  |  Premature ejaculation  |  1
HP:0004757  |  Paroxysmal atrial fibrillation  |  1
HP:0003074  |  High blood glucose  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0001578  |  Hypercortisolism  |  1
HP:0000873  |  Diabetes insipidus  |  1
HP:0001513  |  Obesity  |  1
HP:0005305  |  Cerebral vein thrombosis  |  1
HP:0006554  |  Acute hepatic failure  |  1
HP:0004398  |  Peptic ulcer  |  1
HP:0003546  |  Exercise intolerance  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0001698  |  Pericardial effusions  |  1
HP:0002157  |  Azotaemia  |  1
HP:0002797  |  Increased bone resorption  |  1
HP:0000112  |  Nephropathy  |  1
HP:0100615  |  Neoplasm of the ovary  |  1
HP:0006562  |  Viral hepatitis  |  1
HP:0002493  |  Corticospinal tract dysfunction  |  1
HP:0002905  |  Hyperphosphatemia  |  1
HP:0000078  |  Genital abnormalities  |  1
HP:0100028  |  Abnormal thryoid location  |  1
HP:0001541  |  Ascites  |  1
HP:0000093  |  Proteinuria  |  1
HP:0001045  |  Blotchy loss of skin color  |  1
HP:0011787  |  Central hypothyroidism  |  1
HP:0000738  |  Sensory hallucination  |  1
HP:0002013  |  Emesis  |  1
HP:0002445  |  Paralysis of all four limbs  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0008200  |  Primary hyperparathyroidism  |  1
HP:0002666  |  Pheochromocytoma  |  1
HP:0010741  |  Peripheral edema of lower extremity  |  1
HP:0012251  |  ST segment elevation  |  1
HP:0005987  |  Multinodular goiter  |  1
HP:0000554  |  Uveitis  |  1
HP:0001596  |  Hair loss  |  1
HP:0001259  |  Coma  |  1
HP:0001901  |  Abnormally shaped erythrocytes  |  1
HP:0100246  |  Osteoma  |  1
HP:0002287  |  Progressive alopecia  |  1
HP:0002621  |  Atherosclerosis  |  1
HP:0001337  |  Tremor  |  1
HP:0001909  |  Leukemia  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0001997  |  Gout  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0002516  |  Intracranial pressure elevation  |  1
HP:0003146  |  Decreased circulating cholesterol level  |  1
HP:0000967  |  Petechiae  |  1
HP:0000826  |  Precocious puberty  |  1
HP:0002895  |  Papillary thyroid carcinoma  |  1
HP:0000843  |  Hyperparathyroidism  |  1
HP:0002633  |  Vasculitis  |  1
HP:0008249  |  Large thyroid  |  1
HP:0000833  |  Glucose intolerance  |  1
HP:0002094  |  Dyspnea  |  1
HP:0001993  |  Ketoacidosis  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0002045  |  Abnormally low body temperature  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0003701  |  Proximal limb muscle weakness  |  1
HP:0100660  |  Dyskinesis  |  1
HP:0100539  |  Periorbital swelling  |  1
HP:0002897  |  Parathyroid adenoma  |  1
HP:0100522  |  Thymoma  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0001254  |  Lethargy  |  1
HP:0001271  |  Polyneuropathy  |  1
Disease ID 320
Disease hyperthyroidism
Manually Symptom
UMLS  | Name(Total Manually Symptoms:255)
C2712340  |  dyspnoea
C2712332  |  vomiting
C2712323  |  hypoglycaemia
C2712322  |  tachycardia
C2711227  |  hepatic steatosis
C2700526  |  erythrocytosis
C2678504  |  osteoporosis
C2676454  |  h syndrome
C2364377  |  delirium
C2364324  |  increased intracranial pressure
C2364133  |  infection
C2364118  |  weakness
C2364108  |  stigma
C2364072  |  depression
C2364051  |  fatigue
C2364050  |  hypothermia
C2348360  |  atrial enlargement
C2240374  |  eosinophilia
C2219717  |  amenorrhea
C2203646  |  jaundice
C2186532  |  liver disease
C2108109  |  sinus tachycardia
C2108077  |  atrioventricular block
C2048468  |  male infertility
C2015956  |  throat pain
C1963279  |  viral hepatitis
C1963274  |  vasculitis
C1963235  |  sick sinus syndrome
C1963220  |  pulmonary hypertension
C1963165  |  malabsorption
C1963138  |  hypertension
C1963135  |  hepatic necrosis
C1963120  |  gynecomastia
C1963091  |  diarrhea
C1963064  |  anxiety
C1956391  |  temporal arteritis
C1868682  |  paroxysmal kinesigenic choreoathetosis
C1839141  |  thyroxine-binding globulin deficiency
C1704212  |  embolism
C1619734  |  pulmonary arterial hypertension
C1609519  |  adrenal myelolipoma
C1565489  |  renal insufficiency
C1555754  |  cardiovascular disease
C1527330  |  pyridoxine deficiency
C1522057  |  duodenitis
C1456784  |  paranoid disorder
C1442871  |  craniosynostosis
C1442837  |  myocardial necrosis
C1384672  |  hypoparathyroidism
C1336753  |  thyroid lymphoma
C1330961  |  acidity
C1279412  |  periodic paralysis
C1135191  |  systolic heart failure
C1135188  |  critical illness myopathy
C1059185  |  exophthalmus
C1000483  |  anemia
C0948266  |  latent tetany
C0948008  |  ischemic stroke
C0920157  |  mesenteric ischemia
C0917981  |  progressive spinal muscular atrophy
C0878544  |  cardiomyopathy
C0851578  |  sleep disorders
C0848676  |  male subfertility
C0752303  |  urological manifestations
C0752303  |  urological manifestation
C0752196  |  ballism
C0748159  |  pulmonary involvement
C0743711  |  eye lesion
C0741949  |  cardiovascular pathology
C0740394  |  hyperuricemia
C0700323  |  neuromuscular blockade
C0679466  |  cognitive deficits
C0678222  |  breast cancer
C0600336  |  subcorneal pustular dermatosis
C0600086  |  toxic goiter
C0549473  |  thyroid gland carcinoma
C0549473  |  thyroid carcinoma
C0549473  |  thyroid cancer
C0549473  |  carcinoma of the thyroid
C0549473  |  cancer of the thyroid
C0549124  |  arterial embolism
C0542052  |  coronary insufficiency
C0497327  |  dementia
C0494491  |  mononeuropathy
C0476270  |  cardiovascular symptoms
C0428908  |  sinus node dysfunction
C0427008  |  stiffness
C0426768  |  o sign
C0424755  |  fever
C0422833  |  ent symptoms
C0419203  |  osteopathy
C0410198  |  proximal myopathy
C0400916  |  acute hepatitis e
C0398623  |  hypercoagulable state
C0398623  |  hypercoagulability state
C0376293  |  stigmata
C0342882  |  heterozygous familial hypercholesterolemia
C0342342  |  idiopathic hypoparathyroidism
C0339143  |  thyroid ophthalmopathy
C0338573  |  cerebral venous sinus thrombosis
C0311223  |  frozen shoulder
C0277928  |  venous hum
C0271650  |  impaired glucose tolerance
C0271650  |  glucose intolerance
C0270823  |  petit mal status
C0270739  |  hemichorea
C0270327  |  enuresis
C0268445  |  normokalemic periodic paralysis
C0268283  |  disorders of steroid metabolism
C0267804  |  centrilobular hepatic necrosis
C0266928  |  rapidly progressive periodontitis
C0264886  |  conduction disorders
C0264757  |  rheumatic valvular disease
C0264686  |  coronary embolism
C0262587  |  parathyroid adenoma
C0243050  |  cardiovascular abnormalities
C0242342  |  sheehan's syndrome
C0242292  |  mccune-albright syndrome
C0241885  |  exercise intolerance
C0238462  |  medullary thyroid carcinoma
C0236663  |  alcohol withdrawal syndrome
C0235527  |  right-sided heart failure
C0235527  |  right heart failure
C0235480  |  paroxysmal atrial fibrillation
C0235430  |  ketonaemia
C0235401  |  abnormal glucose tolerance
C0235394  |  wasting
C0235369  |  granulomatous hepatitis
C0235250  |  hyperemesis
C0235169  |  excitability
C0234132  |  pyramidal sign
C0233401  |  psychiatric symptoms
C0233397  |  psychological symptoms
C0232848  |  secondary enuresis
C0232197  |  fibrillation
C0231230  |  fatigability
C0221505  |  cerebral lesions
C0221002  |  primary hyperparathyroidism
C0206682  |  follicular carcinoma
C0206146  |  myocardial stunning
C0162568  |  erythropoietic protoporphyria
C0162565  |  acute intermittent porphyria
C0162316  |  iron deficiency anemia
C0156259  |  renal hypertrophy
C0155301  |  retrobulbar neuritis
C0152171  |  primary pulmonary hypertension
C0152171  |  idiopathic pulmonary hypertension
C0152025  |  polyneuropathy
C0151945  |  cerebral venous thrombosis
C0151798  |  liver necrosis
C0151744  |  myocardial ischemia
C0149670  |  disorders of carbohydrate metabolism
C0085681  |  hyperphosphatemia
C0085681  |  hyperphosphataemia
C0085661  |  onycholysis
C0085655  |  polymyositis
C0085583  |  choreoathetosis
C0043117  |  idiopathic thrombocytopenic purpura
C0043117  |  autoimmune thrombocytopenic purpura
C0042024  |  loss of bladder control
C0041326  |  pleural tuberculosis
C0040149  |  subacute thyroiditis
C0040137  |  thyroid nodules
C0040034  |  thrombocytopenia
C0039621  |  tetany
C0038478  |  struma ovarii
C0038238  |  steatorrhoea
C0038218  |  status asthmaticus
C0038013  |  ankylosing spondylitis
C0037763  |  muscle spasms
C0037672  |  sleepwalking
C0035579  |  rickets
C0035435  |  rheumatism
C0034150  |  purpura
C0034063  |  pulmonary edema
C0033774  |  pruritus
C0033103  |  pretibial myxedema
C0033038  |  premature ejaculation
C0032617  |  polyuria
C0032000  |  pituitary adenomas
C0031117  |  peripheral neuropathy
C0030552  |  muscle pareses
C0030517  |  parathyroid disease
C0030312  |  pancytopenia
C0029458  |  postmenopausal bone loss
C0029132  |  optic neuropathies
C0029089  |  oculomotor paralysis
C0027947  |  neutropenia
C0027868  |  neuromuscular disorders
C0027726  |  nephrotic syndrome
C0027145  |  myxoedema
C0027145  |  myxedema
C0027126  |  myotonic dystrophy
C0027066  |  myoclonus
C0027051  |  myocardial infarction
C0026896  |  myasthenia gravis
C0026848  |  myopathy
C0026848  |  myopathies
C0026848  |  muscular disorders
C0026848  |  muscular diseases
C0026846  |  muscle wasting
C0026650  |  movement disorders
C0026267  |  mitral valve prolapse
C0026266  |  mitral regurgitation
C0025517  |  metabolism disorder
C0025517  |  metabolic disorders
C0024141  |  systemic lupus erythematosus
C0023895  |  hepatic pathology
C0022972  |  lambert-eaton syndrome
C0022354  |  cholestatic jaundice
C0020640  |  hypoprothrombinemia
C0020615  |  hypoglycemia
C0020505  |  hyperphagia
C0020502  |  hyperparathyroidism
C0020456  |  hyperglycemia
C0020437  |  hypercalcemia
C0020437  |  hypercalcaemia
C0020217  |  molar pregnancy
C0019158  |  hepatitis
C0018817  |  atrial septal defect
C0018802  |  congestive heart failure
C0018801  |  heart failure
C0018801  |  cardiac insufficiency
C0018801  |  cardiac failure
C0018799  |  cardiac disorders
C0018794  |  heart block
C0018418  |  gynaecomastia
C0018213  |  graves-basedow disease
C0018213  |  graves' disease
C0018021  |  goitre
C0018021  |  goiter
C0016065  |  polyostotic fibrous dysplasia
C0015300  |  exophthalmos
C0012569  |  diplopia
C0012242  |  digestive diseases
C0011880  |  diabetic ketosis
C0011860  |  diabetes
C0011849  |  diabetes mellitus
C0011168  |  dysphagia
C0010073  |  coronary vasospasm
C0010073  |  coronary artery spasm
C0008497  |  choriocarcinoma
C0008489  |  chorea
C0008372  |  intrahepatic cholestasis
C0008312  |  primary biliary cirrhosis
C0007222  |  cardiovascular disorders
C0007193  |  dilated cardiomyopathy
C0005779  |  blood coagulation disorders
C0005586  |  bipolar disorder
C0004936  |  mental disorders
C0004364  |  autoimmune disorder
C0004245  |  av blocks
C0003811  |  rhythm disorder
C0002892  |  pernicious anaemia
C0001403  |  addison's disease
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:75)
C0018213  |  graves' disease  |  21
C0232197  |  fibrillation  |  16
C0018021  |  goiter  |  14
C0018801  |  heart failure  |  9
C0020538  |  hypertension  |  9
C0011847  |  diabetes  |  6
C0007115  |  thyroid cancer  |  5
C0018021  |  goitre  |  5
C0878544  |  cardiomyopathy  |  4
C0030312  |  pancytopenia  |  4
C0029456  |  osteoporosis  |  4
C0018802  |  congestive heart failure  |  3
C0039231  |  tachycardia  |  3
C0398623  |  hypercoagulable state  |  3
C0030443  |  periodic paralysis  |  3
C0235250  |  hyperemesis  |  3
C0020542  |  pulmonary hypertension  |  3
C0004093  |  weakness  |  3
C0011168  |  dysphagia  |  2
C0040147  |  thyroiditis  |  2
C0020217  |  molar pregnancy  |  2
C0013922  |  embolism  |  2
C0026848  |  muscular disorders  |  2
C0022346  |  jaundice  |  2
C0018801  |  cardiac failure  |  2
C0549473  |  thyroid carcinoma  |  2
C0010278  |  craniosynostosis  |  2
C0020437  |  hypercalcemia  |  2
C0026848  |  myopathy  |  2
C0023895  |  liver disease  |  2
C0009450  |  infection  |  2
C0027051  |  myocardial infarction  |  2
C0497327  |  dementia  |  2
C0011570  |  depression  |  2
C0007222  |  cardiovascular disorders  |  2
C0040137  |  thyroid nodules  |  1
C0221002  |  primary hyperparathyroidism  |  1
C0152025  |  polyneuropathy  |  1
C0085655  |  polymyositis  |  1
C0410198  |  proximal myopathy  |  1
C0020456  |  hyperglycemia  |  1
C0042963  |  vomiting  |  1
C0948008  |  ischemic stroke  |  1
C0085681  |  hyperphosphatemia  |  1
C0027126  |  myotonic dystrophy  |  1
C0426768  |  o sign  |  1
C0042721  |  viral hepatitis  |  1
C0019158  |  hepatitis  |  1
C0151740  |  increased intracranial pressure  |  1
C0020672  |  hypothermia  |  1
C0233401  |  psychiatric symptoms  |  1
C0032000  |  pituitary adenomas  |  1
C0262587  |  parathyroid adenoma  |  1
C0151945  |  cerebral venous thrombosis  |  1
C0002871  |  anemia  |  1
C0241885  |  exercise intolerance  |  1
C0270739  |  hemichorea  |  1
C1527405  |  erythrocytosis  |  1
C0004096  |  asthma  |  1
C0020502  |  hyperparathyroidism  |  1
C0206682  |  follicular carcinoma  |  1
C0339143  |  thyroid ophthalmopathy  |  1
C0026896  |  myasthenia gravis  |  1
C0027145  |  myxedema  |  1
C0235480  |  paroxysmal atrial fibrillation  |  1
C0159069  |  impaired glucose tolerance  |  1
C0042384  |  vasculitis  |  1
C0027868  |  neuromuscular disorders  |  1
C0008489  |  chorea  |  1
C0020505  |  hyperphagia  |  1
C0033038  |  premature ejaculation  |  1
C0235527  |  right heart failure  |  1
C0152171  |  idiopathic pulmonary hypertension  |  1
C0005586  |  bipolar disorder  |  1
C1619734  |  pulmonary arterial hypertension  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs121908873184660767253TSHRumls:C0020550BeFreeInterestingly, an additional constitutively active somatic mutation (S281N) was identified on the second parental TSHR allele of the hyperthyroid index patient.0.1526425452008TSHR;LOC1019284621481139828GA,T
rs178794692296848326191PTPN22umls:C0020550BeFreeEvaluation of genotypes (HLA DRB1*03, DQA1*05, DQB1*02; CTLA4 49A/G, CT60 A/G; PTPN22 C/T) in relation to phenotypes (age, sex, severity (clinical, biochemical, and immunological)) of hyperthyroidism and environmental factors (smoking, stress questionnaires).0.0002714422012HLA-DRB1;LOC105369230632584333CG
rs17879469229684833123HLA-DRB1umls:C0020550BeFreeEvaluation of genotypes (HLA DRB1*03, DQA1*05, DQB1*02; CTLA4 49A/G, CT60 A/G; PTPN22 C/T) in relation to phenotypes (age, sex, severity (clinical, biochemical, and immunological)) of hyperthyroidism and environmental factors (smoking, stress questionnaires).0.0002714422012HLA-DRB1;LOC105369230632584333CG
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:11)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020550carbimazoleD00223122232-54-8hyperthyroidismMESH:D006980therapeutic12549952
C0020550glutathioneD00597870-18-8hyperthyroidismMESH:D006980marker/mechanism19914224
C0020550peginterferon alfa-2aC100416-hyperthyroidismMESH:D006980marker/mechanism18097301
C0020550propranololD011433525-66-6hyperthyroidismMESH:D006980therapeutic11193444
C0020550propylthiouracilD01144151-52-5hyperthyroidismMESH:D006980marker/mechanism12621104
C0020550propylthiouracilD01144151-52-5hyperthyroidismMESH:D006980therapeutic11014318
C0020550reserpineD01211050-55-5hyperthyroidismMESH:D006980therapeutic4589407
C0020550ribavirinD01225436791-04-5hyperthyroidismMESH:D006980marker/mechanism18097301
C0020550rifampinD01229313292-46-1hyperthyroidismMESH:D006980marker/mechanism16236685
C0020550sotalolD0130153930-20-9hyperthyroidismMESH:D006980marker/mechanism83509
C0020550vitamin eD0148101406-18-4hyperthyroidismMESH:D006980therapeutic19914224
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)