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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   thrombocytopenia
  

Disease ID 553
Disease thrombocytopenia
Definition
A subnormal level of BLOOD PLATELETS.
Synonym
platelet count decreased
thrombocytopaenia
thrombocytopenia (disorder)
thrombocytopenia [disease/finding]
thrombocytopenia nos
thrombocytopenia nos (disorder)
thrombocytopenia, nos
thrombocytopenia, unspecified
thrombocytopenias
thrombocytopenic disorder
thrombocytopenic disorder (disorder)
thrombopenia
thrombopenias
DOID
ICD10
UMLS
C0040034
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:244)
C0002871  |  anemia  |  64
C0040053  |  thrombosis  |  40
C0019158  |  hepatitis  |  34
C0002878  |  hemolytic anemia  |  25
C0027947  |  neutropenia  |  25
C0019196  |  hepatitis c  |  25
C0023895  |  liver disease  |  21
C0024141  |  systemic lupus erythematosus  |  18
C0024530  |  malaria  |  15
C0023890  |  cirrhosis  |  15
C0409974  |  lupus erythematosus  |  14
C0002871  |  anaemia  |  12
C0023418  |  leukemia  |  12
C0020532  |  hypersplenism  |  11
C0026986  |  myelodysplastic syndrome  |  9
C0034150  |  purpura  |  8
C0023890  |  liver cirrhosis  |  7
C0023530  |  leucopenia  |  7
C0042769  |  virus infection  |  6
C0155765  |  microangiopathy  |  6
C0007102  |  colon cancer  |  6
C0041296  |  tuberculosis  |  6
C0034065  |  pulmonary embolism  |  5
C0002878  |  haemolytic anaemia  |  5
C0272286  |  immune thrombocytopenia  |  5
C0019100  |  dengue hemorrhagic fever  |  5
C0030312  |  pancytopenia  |  5
C0026986  |  myelodysplastic syndromes  |  5
C0023530  |  leukopenia  |  5
C0017205  |  gaucher disease  |  4
C0023364  |  leptospirosis  |  4
C0024537  |  plasmodium vivax malaria  |  4
C0011847  |  diabetes  |  4
C0034155  |  thrombotic thrombocytopenic purpura  |  4
C0024537  |  vivax malaria  |  4
C0023434  |  chronic lymphocytic leukemia  |  4
C1565489  |  renal insufficiency  |  3
C0162316  |  iron deficiency anemia  |  3
C0042769  |  viral infection  |  3
C0023448  |  lymphocytic leukemia  |  3
C0001824  |  agranulocytosis  |  3
C0032914  |  preeclampsia  |  3
C0015230  |  rash  |  3
C0598894  |  monocytic leukemia  |  3
C0085669  |  acute leukemia  |  3
C0042345  |  varices  |  3
C0085278  |  antiphospholipid syndrome  |  3
C0030312  |  bone marrow failure  |  3
C0024312  |  lymphopenia  |  3
C0023895  |  liver diseases  |  3
C0024299  |  lymphoma  |  3
C0040053  |  thrombus  |  3
C0020541  |  portal hypertension  |  3
C0041327  |  pulmonary tuberculosis  |  3
C0014867  |  esophageal varices  |  3
C0241910  |  autoimmune hepatitis  |  3
C0024535  |  falciparum malaria  |  3
C0033687  |  proteinuria  |  2
C0032285  |  pneumonia  |  2
C0836924  |  thrombocytosis  |  2
C0043194  |  wiskott-aldrich syndrome  |  2
C0023449  |  acute lymphoblastic leukaemia  |  2
C0019196  |  hepatitis c infection  |  2
C0018916  |  hemangiomas  |  2
C0012739  |  disseminated intravascular coagulation  |  2
C0042384  |  vasculitis  |  2
C0020538  |  hypertension  |  2
C0012739  |  consumptive coagulopathy  |  2
C0007570  |  celiac disease  |  2
C0021400  |  influenza  |  2
C0019099  |  crimean-congo hemorrhagic fever  |  2
C0019087  |  hemorrhagic diathesis  |  2
C0376545  |  hematologic malignancies  |  2
C0002880  |  autoimmune haemolytic anaemia  |  2
C0027051  |  myocardial infarct  |  2
C0013595  |  eczema  |  2
C0010346  |  crohn's disease  |  2
C0002880  |  autoimmune hemolytic anemia  |  2
C0008049  |  varicella  |  2
C0010068  |  coronary artery disease  |  2
C0040028  |  essential thrombocythemia  |  2
C0006309  |  brucellosis  |  2
C0024623  |  gastric cancer  |  2
C0043117  |  idiopathic thrombocytopenic purpura  |  2
C0039730  |  thalassemia  |  2
C0019061  |  hemolytic uremic syndrome  |  2
C0026764  |  multiple myeloma  |  2
C0012739  |  consumption coagulopathy  |  2
C0035078  |  renal failure  |  2
C0027051  |  myocardial infarction  |  2
C0011854  |  type 1 diabetes  |  2
C0003864  |  arthritis  |  1
C0024115  |  lung disease  |  1
C0376300  |  dengue shock syndrome  |  1
C0006060  |  boutonneuse fever  |  1
C0024419  |  macroglobulinemia  |  1
C0272126  |  evan's syndrome  |  1
C0015230  |  exanthema  |  1
C0087086  |  thrombi  |  1
C0017636  |  glioblastoma  |  1
C0007115  |  thyroid ca  |  1
C0006663  |  calcinosis  |  1
C0008312  |  biliary cirrhosis  |  1
C0009782  |  connective tissue diseases  |  1
C0009782  |  connective tissue disease  |  1
C0042769  |  viral infections  |  1
C0010692  |  cystitis  |  1
C0036202  |  sarcoidosis  |  1
C0023467  |  acute myelogenous leukemia  |  1
C0029456  |  osteoporosis  |  1
C0026764  |  myeloma  |  1
C0011603  |  dermatitis  |  1
C0009447  |  common variable immunodeficiency  |  1
C0021053  |  immune disorder  |  1
C0019163  |  hepatitis b  |  1
C0272236  |  hyper-igm syndrome  |  1
C0398689  |  x-linked hyper-igm syndrome  |  1
C0022658  |  renal disorders  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C1955861  |  t-lgl leukemia  |  1
C0032285  |  lung inflammation  |  1
C0024299  |  malignant lymphoma  |  1
C0020302  |  congenital glaucoma  |  1
C0034186  |  pyelonephritis  |  1
C0008312  |  primary biliary cirrhosis  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0023418  |  leukemias  |  1
C0031347  |  pharyngeal cancer  |  1
C0011633  |  dermatomyositis  |  1
C0036421  |  systemic sclerosis  |  1
C0007113  |  rectal cancer  |  1
C0025303  |  meningococcal disease  |  1
C0040188  |  tic disorders  |  1
C0013592  |  ectropion  |  1
C0015530  |  factor xiii deficiency  |  1
C0004576  |  babesiosis  |  1
C0010414  |  cryptococcosis  |  1
C0153392  |  nasopharyngeal cancer  |  1
C1145670  |  respiratory failure  |  1
C0018920  |  cavernous hemangiomas  |  1
C0002892  |  pernicious anemia  |  1
C0007642  |  cellulitis  |  1
C0376545  |  hematologic malignancy  |  1
C0033860  |  psoriasis  |  1
C0152021  |  congenital heart disease  |  1
C0039538  |  teratoma  |  1
C0023470  |  myelogenous leukemia  |  1
C0011880  |  diabetic ketoacidosis  |  1
C0018916  |  angioma  |  1
C0270922  |  demyelinating polyneuropathy  |  1
C0685938  |  gastrointestinal cancer  |  1
C0025362  |  mental retardation  |  1
C0398623  |  hypercoagulability state  |  1
C0206062  |  interstitial lung disease  |  1
C0023891  |  alcoholic cirrhosis  |  1
C0398623  |  hypercoagulability  |  1
C0004045  |  birth asphyxia  |  1
C0035309  |  retinopathy  |  1
C0019101  |  hemorrhagic fever with renal syndrome  |  1
C1704437  |  respiratory distress syndrome  |  1
C0242379  |  lung cancer  |  1
C0003507  |  aortic valve stenosis  |  1
C0334634  |  mantle cell lymphoma  |  1
C0020459  |  hyperinsulinism  |  1
C0018920  |  cavernous hemangioma  |  1
C0021053  |  immune disorders  |  1
C0000832  |  placental abruption  |  1
C0018818  |  ventricular septal defect  |  1
C0086543  |  cataract  |  1
C0026654  |  moyamoya disease  |  1
C0405580  |  hypoadrenocorticism  |  1
C0015625  |  fanconi anemia  |  1
C0276688  |  pulmonary cryptococcosis  |  1
C0011991  |  diarrhea  |  1
C0024419  |  waldenstrom's macroglobulinemia  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0040100  |  thymoma  |  1
C0007785  |  cerebral infarct  |  1
C0085692  |  hemorrhagic cystitis  |  1
C0085576  |  microcytic anemia  |  1
C0023788  |  whipple's disease  |  1
C0041331  |  splenic tuberculosis  |  1
C0085411  |  angiodysplasia  |  1
C0022660  |  acute renal failure  |  1
C0085293  |  hepatitis e  |  1
C0014038  |  encephalitis  |  1
C0175703  |  tar syndrome  |  1
C0278883  |  metastatic melanoma  |  1
C0079731  |  b-cell lymphoma  |  1
C0001418  |  adenocarcinoma  |  1
C0376358  |  prostate cancer  |  1
C1261473  |  sarcoma  |  1
C0027022  |  myeloproliferative disorders  |  1
C0009402  |  colorectal cancer  |  1
C0341858  |  adenomyosis  |  1
C0008049  |  varicella infection  |  1
C0023418  |  leukaemia  |  1
C0026654  |  moyamoya  |  1
C0027697  |  nephritis  |  1
C1260402  |  splenic sequestration  |  1
C1140680  |  ovarian cancer  |  1
C0085278  |  anti-phospholipid syndrome  |  1
C0393819  |  chronic inflammatory demyelinating polyneuropathy  |  1
C0272302  |  gray platelet syndrome  |  1
C0041227  |  trypanosomosis  |  1
C0555198  |  malignant glioma  |  1
C0152025  |  polyneuropathy  |  1
C0001623  |  adrenal insufficiency  |  1
C0242584  |  autoimmune thrombocytopenia  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  1
C0032302  |  mycoplasma pneumonia  |  1
C1140680  |  ovarian ca  |  1
C0022661  |  chronic renal failure  |  1
C0014867  |  oesophageal varices  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0027022  |  myeloproliferative disorder  |  1
C0042769  |  viral disease  |  1
C0026934  |  mycoplasma  |  1
C0017601  |  glaucoma  |  1
C0085399  |  ehrlichiosis  |  1
C0856761  |  budd-chiari syndrome  |  1
C0018784  |  sensorineural hearing loss  |  1
C0158761  |  radioulnar synostosis  |  1
C0272126  |  evans' syndrome  |  1
C0010072  |  coronary thrombosis  |  1
C0024419  |  waldenstrom macroglobulinemia  |  1
C0001815  |  myelofibrosis  |  1
C0085278  |  anti-phospholipid antibody syndrome  |  1
C0041466  |  typhoid  |  1
C0007785  |  cerebral infarction  |  1
C0012739  |  disseminated intravascular coagulation (dic)  |  1
C0021053  |  immune disease  |  1
C0002886  |  macrocytic anemia  |  1
C0027059  |  myocarditis  |  1
C0009324  |  ulcerative colitis  |  1
C0019829  |  hodgkin lymphoma  |  1
C0403447  |  chronic renal insufficiency  |  1
C0020538  |  hypertensive disease  |  1
C0032001  |  pituitary apoplexy  |  1
C0034188  |  xanthogranulomatous pyelonephritis  |  1
C0033117  |  priapism  |  1
C0007115  |  thyroid cancer  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:23)
3690  |  ITGB3  |  CTD_human
213  |  ALB  |  CTD_human
1440  |  CSF3  |  CTD_human
4524  |  MTHFR  |  CTD_human
5175  |  PECAM1  |  CTD_human
2623  |  GATA1  |  CTD_human
3440  |  IFNA2  |  CTD_human
3105  |  HLA-A  |  CTD_human
2212  |  FCGR2A  |  CTD_human
9948  |  WDR1  |  CTD_human
2815  |  GP9  |  CTD_human
1437  |  CSF2  |  CTD_human
3562  |  IL3  |  CTD_human
2812  |  GP1BB  |  CTD_human
2120  |  ETV6  |  CLINVAR;CTD_human
7498  |  XDH  |  CTD_human
2056  |  EPO  |  CTD_human
8797  |  TNFRSF10A  |  CTD_human
54205  |  CYCS  |  CTD_human
3704  |  ITPA  |  CTD_human
374569  |  ASPG  |  CTD_human
5196  |  PF4  |  CTD_human
3674  |  ITGA2B  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:34)
54205  |  CYCS  |  CIPHER;CTD_human
2147  |  F2  |  CIPHER
2153  |  F5  |  CIPHER
355  |  FAS  |  CIPHER
356  |  FASLG  |  CIPHER
2212  |  FCGR2A  |  CIPHER;CTD_human
2214  |  FCGR3A  |  CIPHER
2811  |  GP1BA  |  CIPHER
2812  |  GP1BB  |  CIPHER;CTD_human
2814  |  GP5  |  CIPHER
2815  |  GP9  |  CIPHER;CTD_human
3125  |  HLA-DRB3  |  CIPHER
3673  |  ITGA2  |  CIPHER
3674  |  ITGA2B  |  CIPHER;CTD_human
3690  |  ITGB3  |  CIPHER;CTD_human
4524  |  MTHFR  |  CIPHER;CTD_human
4627  |  MYH9  |  CIPHER
26191  |  PTPN22  |  CIPHER
5175  |  PECAM1  |  CTD_human
9948  |  WDR1  |  CTD_human
3562  |  IL3  |  CTD_human
3105  |  HLA-A  |  CTD_human
1437  |  CSF2  |  CTD_human
7498  |  XDH  |  CTD_human
1440  |  CSF3  |  CTD_human
2623  |  GATA1  |  CTD_human
8797  |  TNFRSF10A  |  CTD_human
5196  |  PF4  |  CTD_human
213  |  ALB  |  CTD_human
3704  |  ITPA  |  CTD_human
374569  |  ASPG  |  CTD_human
2120  |  ETV6  |  CTD_human
3440  |  IFNA2  |  CTD_human
2056  |  EPO  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:274)
25  |  ABL1  |  2.391  |  DISEASES
91452  |  ACBD5  |  2.185  |  DISEASES
87  |  ACTN1  |  2.781  |  DISEASES
11093  |  ADAMTS13  |  6.323  |  DISEASES
174  |  AFP  |  2.188  |  DISEASES
204  |  AK2  |  1.635  |  DISEASES
238  |  ALK  |  1.184  |  DISEASES
241  |  ALOX5AP  |  1.006  |  DISEASES
257  |  ALX3  |  1.243  |  DISEASES
22852  |  ANKRD26  |  4.461  |  DISEASES
84071  |  ARMC2  |  1.284  |  DISEASES
171023  |  ASXL1  |  2.176  |  DISEASES
79969  |  ATAT1  |  1.343  |  DISEASES
23545  |  ATP6V0A2  |  1.831  |  DISEASES
567  |  B2M  |  2.955  |  DISEASES
2683  |  B4GALT1  |  2.157  |  DISEASES
685  |  BTC  |  1.398  |  DISEASES
79680  |  C22orf29  |  1.414  |  DISEASES
720  |  C4A  |  1.094  |  DISEASES
721  |  C4B  |  2.554  |  DISEASES
722  |  C4BPA  |  1.983  |  DISEASES
80739  |  C6orf25  |  1.906  |  DISEASES
778  |  CACNA1F  |  1.62  |  DISEASES
285782  |  CAGE1  |  1.213  |  DISEASES
811  |  CALR  |  1.039  |  DISEASES
820  |  CAMP  |  1.307  |  DISEASES
865  |  CBFB  |  1.072  |  DISEASES
388372  |  CCL4L1  |  1.645  |  DISEASES
1232  |  CCR3  |  1.117  |  DISEASES
9332  |  CD163  |  1.585  |  DISEASES
930  |  CD19  |  3.989  |  DISEASES
911  |  CD1C  |  1.365  |  DISEASES
914  |  CD2  |  3.256  |  DISEASES
951  |  CD37  |  1.042  |  DISEASES
958  |  CD40  |  1.987  |  DISEASES
959  |  CD40LG  |  5.807  |  DISEASES
960  |  CD44  |  1.117  |  DISEASES
961  |  CD47  |  1.628  |  DISEASES
921  |  CD5  |  3.647  |  DISEASES
1043  |  CD52  |  3.159  |  DISEASES
966  |  CD59  |  2.462  |  DISEASES
942  |  CD86  |  1.371  |  DISEASES
978  |  CDA  |  2.256  |  DISEASES
1025  |  CDK9  |  1.133  |  DISEASES
1038  |  CDR1  |  1.419  |  DISEASES
1041  |  CDSN  |  1.828  |  DISEASES
629  |  CFB  |  2.387  |  DISEASES
3075  |  CFH  |  3.718  |  DISEASES
10878  |  CFHR3  |  1.924  |  DISEASES
3426  |  CFI  |  3.213  |  DISEASES
1111  |  CHEK1  |  1.483  |  DISEASES
339390  |  CLEC4G  |  1.024  |  DISEASES
8418  |  CMAHP  |  1.723  |  DISEASES
51287  |  COA4  |  1.996  |  DISEASES
1378  |  CR1  |  1.727  |  DISEASES
1380  |  CR2  |  2.409  |  DISEASES
1399  |  CRKL  |  1.361  |  DISEASES
1435  |  CSF1  |  1.495  |  DISEASES
2919  |  CXCL1  |  1.184  |  DISEASES
6387  |  CXCL12  |  1.488  |  DISEASES
2833  |  CXCR3  |  1.095  |  DISEASES
7852  |  CXCR4  |  1.403  |  DISEASES
1576  |  CYP3A4  |  2.275  |  DISEASES
147906  |  DACT3  |  1.027  |  DISEASES
65992  |  DDRGK1  |  1.299  |  DISEASES
51428  |  DDX41  |  3.342  |  DISEASES
11325  |  DDX42  |  2.356  |  DISEASES
1736  |  DKC1  |  1.44  |  DISEASES
28514  |  DLL1  |  2.64  |  DISEASES
3301  |  DNAJA1  |  2.514  |  DISEASES
1791  |  DNTT  |  1.02  |  DISEASES
1806  |  DPYD  |  1.4  |  DISEASES
5169  |  ENPP3  |  2.417  |  DISEASES
30816  |  ERVW-1  |  1.252  |  DISEASES
2113  |  ETS1  |  1.79  |  DISEASES
2120  |  ETV6  |  2.063  |  DISEASES
2159  |  F10  |  2.734  |  DISEASES
2160  |  F11  |  2.16  |  DISEASES
2149  |  F2R  |  2.907  |  DISEASES
2152  |  F3  |  6.392  |  DISEASES
2155  |  F7  |  4.087  |  DISEASES
2157  |  F8  |  3.711  |  DISEASES
389119  |  FAM212A  |  1.869  |  DISEASES
2209  |  FCGR1A  |  2.921  |  DISEASES
2213  |  FCGR2B  |  3.56  |  DISEASES
2214  |  FCGR3A  |  3.261  |  DISEASES
2224  |  FDPS  |  2.776  |  DISEASES
81608  |  FIP1L1  |  1.407  |  DISEASES
2313  |  FLI1  |  2.148  |  DISEASES
2316  |  FLNA  |  1.662  |  DISEASES
2323  |  FLT3LG  |  1.417  |  DISEASES
2290  |  FOXG1  |  3.129  |  DISEASES
50943  |  FOXP3  |  2.213  |  DISEASES
2526  |  FUT4  |  1.788  |  DISEASES
53827  |  FXYD5  |  1.55  |  DISEASES
2534  |  FYN  |  1.076  |  DISEASES
2623  |  GATA1  |  4.336  |  DISEASES
2624  |  GATA2  |  1.812  |  DISEASES
2625  |  GATA3  |  1.831  |  DISEASES
2628  |  GATM  |  2.527  |  DISEASES
8328  |  GFI1B  |  3.097  |  DISEASES
728441  |  GGT2  |  1.995  |  DISEASES
2804  |  GOLGB1  |  1.876  |  DISEASES
2811  |  GP1BA  |  5.296  |  DISEASES
2812  |  GP1BB  |  4.818  |  DISEASES
2875  |  GPT  |  1.157  |  DISEASES
2885  |  GRB2  |  1.694  |  DISEASES
2935  |  GSPT1  |  1.477  |  DISEASES
2993  |  GYPA  |  1.527  |  DISEASES
2994  |  GYPB  |  1.036  |  DISEASES
3030  |  HADHA  |  2.834  |  DISEASES
3039  |  HBA1  |  1.485  |  DISEASES
3043  |  HBB  |  1.459  |  DISEASES
3052  |  HCCS  |  1.192  |  DISEASES
3055  |  HCK  |  1.942  |  DISEASES
10614  |  HEXIM1  |  1.107  |  DISEASES
3105  |  HLA-A  |  1.913  |  DISEASES
3112  |  HLA-DOB  |  1.107  |  DISEASES
51155  |  HN1  |  3.059  |  DISEASES
3240  |  HP  |  3.819  |  DISEASES
60495  |  HPSE2  |  3.271  |  DISEASES
3363  |  HTR7  |  2.073  |  DISEASES
8692  |  HYAL2  |  1.316  |  DISEASES
3418  |  IDH2  |  1.425  |  DISEASES
3451  |  IFNA17  |  1.233  |  DISEASES
3440  |  IFNA2  |  3.917  |  DISEASES
3456  |  IFNB1  |  2.506  |  DISEASES
100885789  |  IFNG-AS1  |  1.744  |  DISEASES
3586  |  IL10  |  3.096  |  DISEASES
3605  |  IL17A  |  2.464  |  DISEASES
112744  |  IL17F  |  1.743  |  DISEASES
3559  |  IL2RA  |  1.381  |  DISEASES
133396  |  IL31RA  |  3.074  |  DISEASES
3563  |  IL3RA  |  1.163  |  DISEASES
3612  |  IMPA1  |  1.131  |  DISEASES
54556  |  ING3  |  1.213  |  DISEASES
3664  |  IRF6  |  2.158  |  DISEASES
3681  |  ITGAD  |  2.577  |  DISEASES
3683  |  ITGAL  |  1.867  |  DISEASES
3684  |  ITGAM  |  2.052  |  DISEASES
23421  |  ITGB3BP  |  1.176  |  DISEASES
3704  |  ITPA  |  2.642  |  DISEASES
3713  |  IVL  |  1.683  |  DISEASES
3716  |  JAK1  |  3.323  |  DISEASES
3717  |  JAK2  |  4.094  |  DISEASES
83700  |  JAM3  |  1.403  |  DISEASES
3725  |  JUN  |  1.31  |  DISEASES
9920  |  KBTBD11  |  3.128  |  DISEASES
3767  |  KCNJ11  |  2.503  |  DISEASES
3792  |  KEL  |  1.288  |  DISEASES
3916  |  LAMP1  |  1.284  |  DISEASES
8825  |  LIN7A  |  2.068  |  DISEASES
4067  |  LYN  |  1.439  |  DISEASES
1130  |  LYST  |  1.194  |  DISEASES
4094  |  MAF  |  1.94  |  DISEASES
23764  |  MAFF  |  1.227  |  DISEASES
4097  |  MAFG  |  2.476  |  DISEASES
7975  |  MAFK  |  1.666  |  DISEASES
23542  |  MAPK8IP2  |  2.617  |  DISEASES
84930  |  MASTL  |  2.349  |  DISEASES
4311  |  MME  |  2.245  |  DISEASES
4352  |  MPL  |  6.362  |  DISEASES
143098  |  MPP7  |  1.457  |  DISEASES
4524  |  MTHFR  |  2.247  |  DISEASES
2475  |  MTOR  |  3.351  |  DISEASES
345778  |  MTX3  |  1.358  |  DISEASES
4602  |  MYB  |  1.194  |  DISEASES
4615  |  MYD88  |  1.11  |  DISEASES
114803  |  MYSM1  |  1.457  |  DISEASES
23218  |  NBEAL2  |  4.569  |  DISEASES
4685  |  NCAM2  |  1.052  |  DISEASES
4698  |  NDUFA5  |  1.057  |  DISEASES
4798  |  NFRKB  |  1.955  |  DISEASES
54475  |  NLE1  |  1.23  |  DISEASES
246734  |  NPCDR1  |  1.029  |  DISEASES
8131  |  NPRL3  |  1.405  |  DISEASES
4893  |  NRAS  |  1.101  |  DISEASES
131870  |  NUDT16  |  2.124  |  DISEASES
84876  |  ORAI1  |  1.561  |  DISEASES
142  |  PARP1  |  1.813  |  DISEASES
100630918  |  PARTICL  |  1.254  |  DISEASES
5091  |  PC  |  1.769  |  DISEASES
23590  |  PDSS1  |  1.315  |  DISEASES
5251  |  PHEX  |  1.929  |  DISEASES
51230  |  PHF20  |  1.543  |  DISEASES
54872  |  PIGG  |  1.425  |  DISEASES
5303  |  PIN4  |  1.294  |  DISEASES
5586  |  PKN2  |  2.037  |  DISEASES
5336  |  PLCG2  |  2.899  |  DISEASES
28227  |  PPP2R3B  |  1.404  |  DISEASES
56980  |  PRDM10  |  1.006  |  DISEASES
5568  |  PRKACG  |  1.247  |  DISEASES
122183  |  PRR20A  |  1.178  |  DISEASES
5663  |  PSEN1  |  2.545  |  DISEASES
5688  |  PSMA7  |  1.108  |  DISEASES
56984  |  PSMG2  |  2.961  |  DISEASES
389362  |  PSMG4  |  1.444  |  DISEASES
9051  |  PSTPIP1  |  1.029  |  DISEASES
374308  |  PTCHD3  |  1.111  |  DISEASES
5743  |  PTGS2  |  1.015  |  DISEASES
5781  |  PTPN11  |  2.323  |  DISEASES
5788  |  PTPRC  |  2.779  |  DISEASES
5795  |  PTPRJ  |  1.649  |  DISEASES
5873  |  RAB27A  |  1.613  |  DISEASES
26064  |  RAI14  |  1.75  |  DISEASES
5900  |  RALGDS  |  2.608  |  DISEASES
22821  |  RASA3  |  2.501  |  DISEASES
9939  |  RBM8A  |  4.762  |  DISEASES
64407  |  RGS18  |  1.609  |  DISEASES
6007  |  RHD  |  3.234  |  DISEASES
7732  |  RNF112  |  2.134  |  DISEASES
6097  |  RORC  |  1.204  |  DISEASES
23322  |  RPGRIP1L  |  2.078  |  DISEASES
113675  |  SDSL  |  1.069  |  DISEASES
6401  |  SELE  |  2.137  |  DISEASES
9037  |  SEMA5A  |  1.058  |  DISEASES
123228  |  SENP8  |  1.386  |  DISEASES
462  |  SERPINC1  |  5.475  |  DISEASES
5345  |  SERPINF2  |  2.836  |  DISEASES
140885  |  SIRPA  |  1.247  |  DISEASES
83650  |  SLC35G5  |  2.197  |  DISEASES
342618  |  SLFN14  |  3.079  |  DISEASES
23583  |  SMUG1  |  1.844  |  DISEASES
8303  |  SNN  |  1.229  |  DISEASES
677806  |  SNORA20  |  2.252  |  DISEASES
6625  |  SNRNP70  |  1.67  |  DISEASES
6693  |  SPN  |  2.347  |  DISEASES
84727  |  SPSB2  |  1.778  |  DISEASES
6714  |  SRC  |  2.338  |  DISEASES
6427  |  SRSF2  |  1.303  |  DISEASES
6772  |  STAT1  |  1.347  |  DISEASES
57620  |  STIM2  |  1.053  |  DISEASES
2054  |  STX2  |  3.178  |  DISEASES
6850  |  SYK  |  2.707  |  DISEASES
6888  |  TALDO1  |  2.083  |  DISEASES
54790  |  TET2  |  4.394  |  DISEASES
7018  |  TF  |  1.941  |  DISEASES
7037  |  TFRC  |  1.929  |  DISEASES
7056  |  THBD  |  3.675  |  DISEASES
29087  |  THYN1  |  1.333  |  DISEASES
7072  |  TIA1  |  1.096  |  DISEASES
1678  |  TIMM8A  |  1.4  |  DISEASES
7086  |  TKT  |  1.379  |  DISEASES
7099  |  TLR4  |  1.535  |  DISEASES
51284  |  TLR7  |  1.05  |  DISEASES
54106  |  TLR9  |  1.12  |  DISEASES
7124  |  TNF  |  3.636  |  DISEASES
7133  |  TNFRSF1B  |  1.295  |  DISEASES
8718  |  TNFRSF25  |  2.832  |  DISEASES
10673  |  TNFSF13B  |  2.634  |  DISEASES
7150  |  TOP1  |  4.31  |  DISEASES
127262  |  TPRG1L  |  1.5  |  DISEASES
9322  |  TRIP10  |  1.069  |  DISEASES
55621  |  TRMT1  |  1.775  |  DISEASES
51393  |  TRPV2  |  1.373  |  DISEASES
54970  |  TTC12  |  1.496  |  DISEASES
203068  |  TUBB  |  1.768  |  DISEASES
9898  |  UBAP2L  |  1.046  |  DISEASES
7357  |  UGCG  |  1.594  |  DISEASES
26019  |  UPF2  |  1.23  |  DISEASES
65110  |  UPF3A  |  1.382  |  DISEASES
7390  |  UROS  |  2.364  |  DISEASES
6843  |  VAMP1  |  1.239  |  DISEASES
7422  |  VEGFA  |  3.14  |  DISEASES
7433  |  VIPR1  |  1.264  |  DISEASES
8876  |  VNN1  |  1.629  |  DISEASES
7454  |  WAS  |  5.659  |  DISEASES
23038  |  WDTC1  |  4.934  |  DISEASES
7456  |  WIPF1  |  1.958  |  DISEASES
51741  |  WWOX  |  1.021  |  DISEASES
285525  |  YIPF7  |  1.08  |  DISEASES
161882  |  ZFPM1  |  3.328  |  DISEASES
7750  |  ZMYM2  |  1.294  |  DISEASES
197320  |  ZNF778  |  2.194  |  DISEASES
Locus(Waiting for update.)
Disease ID 553
Disease thrombocytopenia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:206)
HP:0001945  |  Fever  |  194
HP:0001903  |  Anemia  |  80
HP:0012115  |  Liver inflammation  |  34
HP:0001878  |  Haemolytic anaemia  |  32
HP:0001875  |  Neutropenia  |  28
HP:0001744  |  Splenomegaly  |  21
HP:0200123  |  Chronic liver inflammation  |  20
HP:0002725  |  Systemic lupus erythematosus  |  18
HP:0001394  |  Hepatic cirrhosis  |  16
HP:0100806  |  Sepsis  |  15
HP:0001902  |  Giant platelets  |  13
HP:0001909  |  Leukemia  |  12
HP:0001971  |  Hypersplenism  |  12
HP:0003256  |  Coagulopathy  |  11
HP:0002863  |  Myelodysplastic syndrome  |  10
HP:0001892  |  Bleeding diathesis  |  9
HP:0002664  |  Neoplasia  |  8
HP:0000979  |  Purpura  |  8
HP:0001937  |  Microangiopathic hemolytic anemia  |  8
HP:0005537  |  Small platelet size  |  7
HP:0003003  |  Colon cancer  |  7
HP:0002239  |  Gastrointestinal hemorrhage  |  6
HP:0002584  |  Intestinal hemorrhage  |  6
HP:0002170  |  Intracranial hemorrhage  |  6
HP:0011877  |  Increased mean platelet volume  |  6
HP:0001973  |  Autoimmune thrombocytopenia  |  6
HP:0001882  |  Decreased blood leukocyte number  |  5
HP:0001890  |  Autoimmune hemolytic anemia  |  5
HP:0001876  |  Low blood cell count  |  5
HP:0000083  |  Renal insufficiency  |  5
HP:0002721  |  Immunodeficiency  |  5
HP:0003613  |  Antiphospholipid antibodies  |  4
HP:0002249  |  Melena  |  4
HP:0001974  |  Leukocytosis  |  4
HP:0005528  |  Bone marrow hypoplasia  |  4
HP:0005550  |  Chronic lymphatic leukemia  |  4
HP:0002204  |  Pulmonary embolism  |  4
HP:0001409  |  Portal hypertension  |  4
HP:0000822  |  Hypertension  |  4
HP:0002045  |  Abnormally low body temperature  |  4
HP:0003974  |  Absent ossification/absence of radius  |  3
HP:0001891  |  Iron-deficiency anemia  |  3
HP:0000421  |  Bloody nose  |  3
HP:0005521  |  Disseminated intravascular coagulation  |  3
HP:0001895  |  Normochromic anemia  |  3
HP:0002960  |  Autoimmune condition  |  3
HP:0002488  |  Acute leukemias  |  3
HP:0001511  |  Prenatal onset growth retardation  |  3
HP:0002090  |  Pneumonia  |  3
HP:0002719  |  infections, recurrent  |  3
HP:0012234  |  Agranulocytosis  |  3
HP:0002910  |  Elevated transaminases  |  3
HP:0100033  |  Tic disorder  |  3
HP:0003281  |  Increased ferritin  |  3
HP:0001433  |  Enlarged liver and spleen  |  3
HP:0001888  |  Lymphocytopenia  |  3
HP:0012325  |  Chronic myelomonocytic leukemia  |  3
HP:0100602  |  Pre-eclampsia  |  3
HP:0001297  |  Cerebral vascular events  |  3
HP:0001399  |  Liver failure  |  3
HP:0002665  |  Lymphoma  |  3
HP:0001894  |  Thrombocytosis  |  3
HP:0012531  |  Pain  |  3
HP:0001410  |  Decreased liver function  |  2
HP:0002633  |  Vasculitis  |  2
HP:0000964  |  Eczema  |  2
HP:0100626  |  Chronic hepatic failure  |  2
HP:0001919  |  Acute renal failure  |  2
HP:0001658  |  Myocardial infarction  |  2
HP:0002900  |  Hypokalemia  |  2
HP:0001643  |  Persistent ductus arteriosus  |  2
HP:0002625  |  Blood clot in a deep vein  |  2
HP:0005575  |  Hemolytic-uremic syndrome  |  2
HP:0001981  |  Schistocytosis  |  2
HP:0002608  |  Celiac disease  |  2
HP:0008151  |  Prolonged prothrombin time  |  2
HP:0012378  |  Fatigue  |  2
HP:0011874  |  Heparin-induced thrombocytopenia  |  2
HP:0001907  |  Thromboembolic disease  |  2
HP:0001873  |  Low platelet count  |  2
HP:0012311  |  High blood monocyte number  |  2
HP:0100280  |  Morbus Crohn  |  2
HP:0001677  |  Coronary artery disease  |  2
HP:0002240  |  Enlarged liver  |  2
HP:0011273  |  Unequal size of red blood cells  |  2
HP:0003326  |  Muscle pain  |  2
HP:0009829  |  Phocomelia  |  2
HP:0002904  |  High blood bilirubin levels  |  2
HP:0012126  |  Gastric cancer  |  2
HP:0000093  |  Proteinuria  |  2
HP:0012189  |  Hodgkin disease  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  1
HP:0100279  |  Ulcerative colitis  |  1
HP:0006562  |  Viral hepatitis  |  1
HP:0002908  |  Conjugated hyperbilirubinemia  |  1
HP:0001249  |  Mental retardation  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0200058  |  Angiosarcoma  |  1
HP:0002315  |  Headaches  |  1
HP:0001953  |  Diabetic ketosis  |  1
HP:0002018  |  Nausea  |  1
HP:0002901  |  Hypocalcemia  |  1
HP:0040187  |  Neonatal sepsis  |  1
HP:0001369  |  Arthritis  |  1
HP:0000924  |  Abnormality of the skeletal system  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0001048  |  Cavernous angioma  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0003765  |  Psoriasis  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0002613  |  Biliary cirrhosis  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0012330  |  Pyelonephritis  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0000505  |  Poor vision  |  1
HP:0001271  |  Polyneuropathy  |  1
HP:0000716  |  Depression  |  1
HP:0011674  |  Cardiac teratoma  |  1
HP:0002615  |  Low blood pressure  |  1
HP:0004420  |  Arterial thrombosis  |  1
HP:0001650  |  Valvular aortic stenosis  |  1
HP:0000967  |  Petechiae  |  1
HP:0030731  |  Carcinoma  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0005508  |  Waldenstrom macroglobulinemia  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0005520  |  Chronic disseminated intravascular coagulation  |  1
HP:0000790  |  Hematuria  |  1
HP:0004447  |  Poikilocytosis  |  1
HP:0002829  |  Arthralgias  |  1
HP:0000846  |  Hypoadrenalism  |  1
HP:0011419  |  Abruptio placentae  |  1
HP:0000103  |  Polyuria  |  1
HP:0002527  |  Falls  |  1
HP:0000501  |  Glaucoma  |  1
HP:0005547  |  Myeloproliferative disorder  |  1
HP:0008071  |  Maternal hypertension  |  1
HP:0011854  |  Hemoperitoneum  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0001087  |  Childhood glaucoma  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0004844  |  Coombs-positive hemolytic anemia  |  1
HP:0000518  |  Cataract  |  1
HP:0100761  |  Visceral angiomatosis  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0001897  |  Normocytic anemia  |  1
HP:0002329  |  Drowsiness  |  1
HP:0003075  |  Hypoproteinemia  |  1
HP:0009792  |  Teratoma  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0001629  |  Ventricular septal defects  |  1
HP:0012329  |  Angioblastoma  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0003565  |  Elevated sedimentation rate  |  1
HP:0002878  |  Respiratory failure  |  1
HP:0010972  |  Anemia of inadequate production  |  1
HP:0002155  |  Increased triglycerides  |  1
HP:0000656  |  Ectropion  |  1
HP:0000519  |  Cataracts, lenticular, bilateral  |  1
HP:0003761  |  Calcinosis  |  1
HP:0000969  |  Dropsy  |  1
HP:0002014  |  Diarrhea  |  1
HP:0006530  |  Interstitial lung disease  |  1
HP:0008282  |  Unconjugated hyperbilirubinemia  |  1
HP:0002013  |  Emesis  |  1
HP:0004419  |  Recurrent thrombosis  |  1
HP:0000407  |  sensorineural hearing loss  |  1
HP:0001923  |  Reticulocytosis  |  1
HP:0001993  |  Ketoacidosis  |  1
HP:0003401  |  Paresthesia  |  1
HP:0011896  |  Subconjunctival hemorrhage  |  1
HP:0430007  |  Symblepharon  |  1
HP:0012211  |  Renal functional abnormality  |  1
HP:0001541  |  Ascites  |  1
HP:0200119  |  Acute liver inflammation  |  1
HP:0100309  |  Subdural hemorrhage  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0002383  |  Encephalitis  |  1
HP:0000988  |  Exanthem  |  1
HP:0002835  |  Aspiration  |  1
HP:0002093  |  progressive respiratory failure  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0000155  |  Oral ulcer  |  1
HP:0001259  |  Coma  |  1
HP:0002653  |  Bone pain  |  1
HP:0100724  |  Hypercoagulability  |  1
HP:0030746  |  Intraventricular hemorrhage  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0001824  |  Weight loss  |  1
HP:0200023  |  Priapism  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0001972  |  Macrocytic anemia  |  1
HP:0002974  |  Fused forearm bones  |  1
HP:0005110  |  Atrial fibrillation  |  1
HP:0000123  |  Nephritis  |  1
HP:0100843  |  Glioblastoma  |  1
HP:0009733  |  Glioma  |  1
HP:0100242  |  Sarcoma  |  1
HP:0005202  |  Helicobacter pylori infection  |  1
HP:0001935  |  Microcytic anemia  |  1
HP:0000939  |  Osteoporosis  |  1
HP:0000132  |  Hypermenorrhea  |  1
HP:0008207  |  Addison's disease  |  1
Disease ID 553
Disease thrombocytopenia
Manually Symptom
UMLS  | Name(Total Manually Symptoms:82)
C2707258  |  infections
C2697310  |  sarcoidosis
C2364133  |  infection
C2364050  |  hypothermia
C2186532  |  liver disease
C1962966  |  retinopathy
C1962958  |  hematoma
C1660219  |  analgesia
C1623038  |  cirrhosis
C1521999  |  acute myocardial infarction
C1509147  |  histiocytoma
C1508749  |  capillary fragility
C1443043  |  myeloproliferative syndromes
C1387528  |  acute hemolytic anemia
C1384590  |  hemangiomatosis
C1333817  |  giant hemangioma
C1275974  |  splenic hamartoma
C1275974  |  hamartoma of spleen
C1268935  |  microangiopathic hemolytic anemia
C1142517  |  lupus anticoagulant
C1027109  |  scleroderma
C0948824  |  hemorrhagic anemia
C0948089  |  acute coronary syndrome
C0917798  |  cerebral ischemia
C0878643  |  epiphenomenon
C0796110  |  w syndrome
C0796095  |  c syndrome
C0728731  |  prematurity
C0685201  |  splenic hemangioma
C0600502  |  hemostatic disorders
C0398686  |  primary immunodeficiency
C0346424  |  splenic angiosarcoma
C0338575  |  sagittal sinus thrombosis
C0334121  |  inflammatory myofibroblastic tumor
C0282607  |  vascular tumors
C0272412  |  splenic abscess
C0267373  |  intestinal bleeding
C0265053  |  lower extremity thrombophlebitis
C0221025  |  kasabach-merritt syndrome
C0221021  |  microangiopathic haemolytic anaemia
C0206255  |  malaria
C0152915  |  disseminated tuberculosis
C0151945  |  cerebral vein thrombosis
C0085669  |  acute leukemia
C0085278  |  antiphospholipid syndrome
C0042974  |  von willebrand's disease
C0040156  |  thyrotoxicosis
C0040053  |  thrombosis
C0035021  |  relapsing fever
C0034150  |  purpuras
C0034150  |  purpura
C0032285  |  pneumonia
C0032001  |  pituitary apoplexy
C0031256  |  petechiae
C0029927  |  ovarian cyst
C0029166  |  oral manifestations
C0027051  |  myocardial infarction
C0026848  |  myopathy
C0026691  |  kawasaki disease
C0023794  |  lipidosis
C0023418  |  leukemia
C0021051  |  immunodeficiency disorder
C0021051  |  immunodeficiency
C0020532  |  hypersplenism
C0019693  |  hiv infection
C0019618  |  histiocytosis
C0019189  |  chronic hepatitis
C0019101  |  hemorrhagic fever with renal syndrome
C0019087  |  hemorrhagic diathesis
C0019087  |  haemorrhagic diathesis
C0019080  |  hemorrhage
C0018916  |  hemangiomas
C0018916  |  hemangioma
C0017181  |  gastrointestinal hemorrhage
C0010823  |  cmv infection
C0006309  |  brucellosis
C0005956  |  bone marrow disease
C0005818  |  platelet disorders
C0005818  |  blood platelet disorders
C0005779  |  coagulopathy
C0002879  |  acquired hemolytic anemia
C0002878  |  hemolytic anemia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:40)
C0040053  |  thrombosis  |  41
C0009450  |  infection  |  31
C0002878  |  hemolytic anemia  |  27
C0019080  |  hemorrhage  |  22
C0023895  |  liver disease  |  22
C0019189  |  chronic hepatitis  |  20
C0023890  |  cirrhosis  |  16
C0024530  |  malaria  |  15
C0796095  |  c syndrome  |  15
C0023418  |  leukemia  |  12
C0020532  |  hypersplenism  |  12
C0005779  |  coagulopathy  |  11
C0221021  |  microangiopathic hemolytic anemia  |  8
C0034150  |  purpura  |  8
C0021311  |  infections  |  7
C0267373  |  intestinal bleeding  |  6
C0948089  |  acute coronary syndrome  |  5
C0020672  |  hypothermia  |  4
C0085278  |  antiphospholipid syndrome  |  3
C0021051  |  immunodeficiency  |  3
C0398686  |  primary immunodeficiency  |  3
C0032285  |  pneumonia  |  3
C0085669  |  acute leukemia  |  3
C0006309  |  brucellosis  |  2
C0027051  |  myocardial infarction  |  2
C0221021  |  microangiopathic haemolytic anaemia  |  2
C0018916  |  hemangiomas  |  2
C0019087  |  hemorrhagic diathesis  |  2
C0035309  |  retinopathy  |  1
C0728731  |  prematurity  |  1
C0085240  |  lupus anticoagulant  |  1
C0346424  |  splenic angiosarcoma  |  1
C0221025  |  kasabach-merritt syndrome  |  1
C0031256  |  petechiae  |  1
C0032001  |  pituitary apoplexy  |  1
C0019101  |  hemorrhagic fever with renal syndrome  |  1
C0018944  |  hematoma  |  1
C0010823  |  cmv infection  |  1
C0021051  |  immunodeficiency disorder  |  1
C0036202  |  sarcoidosis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs786205154NA2120ETV6umls:C0040034CLINVARNA0.24NAETV61211885921AACAG-
rs786205155NA2120ETV6umls:C0040034CLINVARNA0.24NAETV61211884481TC
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.)
Disease ID 553
Disease thrombocytopenia
Case(Waiting for update.)