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Pediatric Disease Annotations & Medicines



   hemolytic anemia
  

Disease ID 329
Disease hemolytic anemia
Definition
A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES).
Synonym
[x]haemolytic anaemias
[x]hemolytic anemias
[x]hemolytic anemias (disorder)
anaemia haemolytic
anemia hemolytic
anemia hemolytic (nos)
anemia, hemolytic
anemia, hemolytic [disease/finding]
haemolytic anaemia
haemolytic anaemias
haemolytic anaemias nos
hemolytic anemia (disorder)
hemolytic anemia (nos)
hemolytic anemia, nos
hemolytic anemias
hemolytic anemias nos
hemolytic anemias nos (disorder)
increased hemolysis
DOID
UMLS
C0002878
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:153)
C0040034  |  thrombocytopenia  |  27
C0019158  |  hepatitis  |  14
C0035078  |  renal failure  |  9
C0024530  |  malaria  |  7
C0023448  |  lymphocytic leukemia  |  7
C0017920  |  glucose-6-phosphate dehydrogenase deficiency  |  7
C0032285  |  pneumonia  |  7
C0024299  |  lymphoma  |  6
C0023434  |  chronic lymphocytic leukemia  |  6
C0039730  |  thalassemia  |  6
C0020538  |  hypertension  |  6
C0023418  |  leukemia  |  6
C0020542  |  pulmonary hypertension  |  5
C0034150  |  purpura  |  5
C0017920  |  g6pd deficiency  |  5
C0032302  |  mycoplasma pneumonia  |  4
C0026934  |  mycoplasma  |  4
C0002871  |  anemia  |  4
C0022660  |  acute renal failure  |  4
C0032285  |  pneumoniae  |  3
C0272286  |  immune thrombocytopenia  |  3
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  3
C0019061  |  hemolytic uremic syndrome  |  3
C0023530  |  leukopenia  |  3
C0025637  |  methemoglobinemia  |  3
C0155765  |  microangiopathy  |  3
C0024141  |  systemic lupus erythematosus  |  3
C0085278  |  antiphospholipid syndrome  |  3
C0041296  |  tuberculosis  |  3
C0272126  |  evans syndrome  |  3
C0026986  |  myelodysplastic syndrome  |  3
C0019048  |  hemoglobinuria  |  3
C0026764  |  multiple myeloma  |  3
C0034155  |  thrombotic thrombocytopenic purpura  |  2
C0019196  |  hepatitis c  |  2
C0026764  |  myeloma  |  2
C0030312  |  pancytopenia  |  2
C0009324  |  ulcerative colitis  |  2
C0019045  |  hemoglobinopathies  |  2
C0006142  |  breast cancer  |  2
C0004576  |  babesiosis  |  2
C0409974  |  lupus erythematosus  |  2
C0009319  |  colitis  |  2
C0040053  |  thrombus  |  2
C0948201  |  alloimmunization  |  2
C0042384  |  vasculitis  |  2
C0019829  |  hodgkin's lymphoma  |  2
C0042769  |  virus infection  |  2
C0012739  |  disseminated intravascular coagulation  |  2
C0004134  |  ataxia  |  2
C0023890  |  cirrhosis  |  2
C1527336  |  sjogren's syndrome  |  2
C0270612  |  leukoencephalopathy  |  1
C0002895  |  sickle cell disease  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0085436  |  cryptococcal meningitis  |  1
C0398623  |  hypercoagulable state  |  1
C0042870  |  vitamin d defic  |  1
C0030305  |  pancreatitis  |  1
C0021053  |  immune disease  |  1
C0085786  |  idiopathic interstitial pneumonia  |  1
C0012739  |  disseminated intravascular coagulation (dic)  |  1
C0039730  |  thalassemias  |  1
C0042847  |  vitamin b12 defic  |  1
C0000744  |  acanthocytosis  |  1
C0022661  |  end-stage renal failure  |  1
C0013592  |  ectropion  |  1
C0024535  |  falciparum malaria  |  1
C0085273  |  parvovirus b19 infection  |  1
C0008350  |  gallstones  |  1
C0024302  |  large cell lymphoma  |  1
C0029106  |  opisthorchiasis  |  1
C0037998  |  splenic infarction  |  1
C0008350  |  gall stone  |  1
C0020532  |  hypersplenism  |  1
C0020541  |  portal hypertension  |  1
C0007194  |  hypertrophic obstructive cardiomyopathy  |  1
C0027873  |  neuromyelitis optica  |  1
C0019163  |  hepatitis b  |  1
C0012739  |  consumptive coagulopathy  |  1
C0007570  |  celiac disease  |  1
C1266119  |  solitary fibrous tumor  |  1
C0009447  |  common variable immunodeficiency  |  1
C0037928  |  myelopathy  |  1
C0235974  |  pancreatic cancer  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0014118  |  endocarditis  |  1
C0341335  |  cytomegalovirus colitis  |  1
C0241910  |  autoimmune hepatitis  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0023467  |  acute myeloid leukemia  |  1
C0037889  |  hereditary spherocytosis  |  1
C1140680  |  ovarian cancer  |  1
C0041316  |  tuberculous lymphadenitis  |  1
C0022658  |  renal disease  |  1
C0040381  |  tolosa-hunt syndrome  |  1
C0023890  |  liver cirrhosis  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0242584  |  autoimmune thrombocytopenia  |  1
C0027022  |  myeloproliferative disorders  |  1
C0007787  |  transient ischemic attack  |  1
C0017636  |  glioblastoma  |  1
C0040053  |  thrombosis  |  1
C0020550  |  hyperthyroidism  |  1
C0001418  |  adenocarcinoma  |  1
C0040100  |  thymoma  |  1
C0398623  |  hypercoagulability  |  1
C0024205  |  lymphadenitis  |  1
C0008313  |  sclerosing cholangitis  |  1
C0349632  |  splenic marginal zone lymphoma  |  1
C0022672  |  acute tubular necrosis  |  1
C0263666  |  juvenile dermatomyositis  |  1
C0278701  |  gastric adenocarcinoma  |  1
C1565489  |  renal insufficiency  |  1
C0023470  |  myeloid leukemia  |  1
C0011991  |  diarrhea  |  1
C0085642  |  livedo reticularis  |  1
C0012236  |  digeorge syndrome  |  1
C0025289  |  meningitis  |  1
C0034902  |  pure red cell aplasia  |  1
C0546837  |  oesophageal cancer  |  1
C0008728  |  churg-strauss syndrome  |  1
C0023530  |  leucopenia  |  1
C0018801  |  cardiac failure  |  1
C0087086  |  thrombi  |  1
C0023486  |  prolymphocytic leukemia  |  1
C0004135  |  ataxia telangiectasia  |  1
C0024305  |  non-hodgkin's lymphoma  |  1
C0027022  |  myeloproliferative disorder  |  1
C1621958  |  glioblastoma multiforme  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0042847  |  vitamin b12 deficiency  |  1
C1140680  |  ovarian ca  |  1
C0026691  |  kawasaki disease  |  1
C0008311  |  cholangitis  |  1
C0027947  |  neutropenia  |  1
C0001339  |  acute pancreatitis  |  1
C1955861  |  t-lgl leukemia  |  1
C0034902  |  pure red-cell aplasia  |  1
C0023418  |  leukemias  |  1
C0010346  |  crohn's disease  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0027765  |  neurologic disorder  |  1
C0018916  |  hemangioma  |  1
C1527336  |  sjogren syndrome  |  1
C0340968  |  pyruvate kinase deficiency  |  1
C0022353  |  neonatal jaundice  |  1
C0007194  |  obstructive cardiomyopathy  |  1
C0014859  |  esophageal cancer  |  1
C0019829  |  hodgkin lymphoma  |  1
C0032708  |  porphyria  |  1
C0028242  |  nocardiosis  |  1
C0017658  |  glomerulonephritis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:45)
SLC2A1  |  6513  |  UniProtKB-KW
TPI1  |  7167  |  CTD_human;UniProtKB-KW
AK1  |  203  |  UniProtKB-KW
CDAN1  |  146059  |  UniProtKB-KW;GHR
HMOX1  |  3162  |  CTD_human
HBB  |  3043  |  CLINVAR;UniProtKB-KW
LPIN2  |  9663  |  UniProtKB-KW
PIGA  |  5277  |  GHR
G6PD  |  2539  |  CTD_human;UniProtKB-KW
ADA  |  100  |  UniProtKB-KW
KCNN4  |  3783  |  UniProtKB-KW
CD59  |  966  |  UniProtKB-KW
GSS  |  2937  |  UniProtKB-KW
ACSL4  |  2182  |  UniProtKB-KW
IFNA2  |  3440  |  CTD_human
GPI  |  2821  |  CTD_human;UniProtKB-KW
EPO  |  2056  |  CTD_human
SPTA1  |  6708  |  UniProtKB-KW;GHR
C3  |  718  |  UniProtKB-KW
AMMECR1  |  9949  |  UniProtKB-KW
DGKE  |  8526  |  UniProtKB-KW
HBA1  |  3039  |  UniProtKB-KW
HBA2  |  3040  |  UniProtKB-KW
SLC4A1  |  6521  |  CTD_human;UniProtKB-KW;GHR
CFB  |  629  |  UniProtKB-KW
SEC23B  |  10483  |  UniProtKB-KW;GHR
GCLC  |  2729  |  CTD_human;UniProtKB-KW
CFH  |  3075  |  UniProtKB-KW
CFI  |  3426  |  UniProtKB-KW
ITPA  |  3704  |  CTD_human
PGK1  |  5230  |  UniProtKB-KW
CFHR5  |  81494  |  UniProtKB-KW
CD46  |  4179  |  UniProtKB-KW
EPB42  |  2038  |  UniProtKB-KW;GHR
GSR  |  2936  |  CTD_human
RHAG  |  6005  |  UniProtKB-KW
THBD  |  7056  |  UniProtKB-KW
PKLR  |  5313  |  UniProtKB-KW
SPTB  |  6710  |  CTD_human;UniProtKB-KW;GHR
ALDOA  |  226  |  UniProtKB-KW
KLF1  |  10661  |  UniProtKB-KW
EPB41  |  2035  |  UniProtKB-KW
BPGM  |  669  |  UniProtKB-KW
ANK1  |  286  |  UniProtKB-KW;GHR
PIEZO1  |  9780  |  UniProtKB-KW
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
3704  |  ITPA  |  infer
2539  |  G6PD  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:555)
9957  |  HS3ST1  |  DISEASES
3937  |  LCP2  |  DISEASES
933  |  CD22  |  DISEASES
3385  |  ICAM3  |  DISEASES
9488  |  PIGB  |  DISEASES
10077  |  TSPAN32  |  DISEASES
3049  |  HBQ1  |  DISEASES
6128  |  RPL6  |  DISEASES
8079  |  MLF2  |  DISEASES
1738  |  DLD  |  DISEASES
368  |  ABCC6  |  DISEASES
350  |  APOH  |  DISEASES
55644  |  OSGEP  |  DISEASES
7414  |  VCL  |  DISEASES
7593  |  MZF1  |  DISEASES
112755  |  STX1B  |  DISEASES
5434  |  POLR2E  |  DISEASES
129138  |  ANKRD54  |  DISEASES
10042  |  HMGXB4  |  DISEASES
3162  |  HMOX1  |  DISEASES
4627  |  MYH9  |  DISEASES
5283  |  PIGH  |  DISEASES
4792  |  NFKBIA  |  DISEASES
2937  |  GSS  |  DISEASES
51285  |  RASL12  |  DISEASES
26258  |  BLOC1S6  |  DISEASES
1666  |  DECR1  |  DISEASES
2936  |  GSR  |  DISEASES
166  |  AES  |  DISEASES
973  |  CD79A  |  DISEASES
2057  |  EPOR  |  DISEASES
57817  |  HAMP  |  DISEASES
6804  |  STX1A  |  DISEASES
5054  |  SERPINE1  |  DISEASES
727  |  C5  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
40  |  ASIC2  |  DISEASES
6347  |  CCL2  |  DISEASES
952  |  CD38  |  DISEASES
3558  |  IL2  |  DISEASES
3732  |  CD82  |  DISEASES
6688  |  SPI1  |  DISEASES
4254  |  KITLG  |  DISEASES
420  |  ART4  |  DISEASES
3458  |  IFNG  |  DISEASES
2597  |  GAPDH  |  DISEASES
7167  |  TPI1  |  DISEASES
57379  |  AICDA  |  DISEASES
2729  |  GCLC  |  DISEASES
80329  |  ULBP1  |  DISEASES
6206  |  RPS12  |  DISEASES
6908  |  TBP  |  DISEASES
3565  |  IL4  |  DISEASES
7903  |  ST8SIA4  |  DISEASES
80325  |  ABTB1  |  DISEASES
13  |  AADAC  |  DISEASES
7035  |  TFPI  |  DISEASES
4759  |  NEU2  |  DISEASES
5657  |  PRTN3  |  DISEASES
1179  |  CLCA1  |  DISEASES
6402  |  SELL  |  DISEASES
10971  |  YWHAQ  |  DISEASES
51747  |  LUC7L3  |  DISEASES
8161  |  COIL  |  DISEASES
23397  |  NCAPH  |  DISEASES
847  |  CAT  |  DISEASES
140690  |  CTCFL  |  DISEASES
5335  |  PLCG1  |  DISEASES
1088  |  CEACAM8  |  DISEASES
8192  |  CLPP  |  DISEASES
718  |  C3  |  DISEASES
5199  |  CFP  |  DISEASES
92797  |  HELB  |  DISEASES
57576  |  KIF17  |  DISEASES
10365  |  KLF2  |  DISEASES
10875  |  FGL2  |  DISEASES
2678  |  GGT1  |  DISEASES
53947  |  A4GALT  |  DISEASES
2658  |  GDF2  |  DISEASES
9526  |  MPDU1  |  DISEASES
9084  |  VCY  |  DISEASES
353513  |  VCY1B  |  DISEASES
6217  |  RPS16  |  DISEASES
3040  |  HBA2  |  DISEASES
25943  |  C20orf194  |  DISEASES
4695  |  NDUFA2  |  DISEASES
2056  |  EPO  |  DISEASES
3050  |  HBZ  |  DISEASES
8666  |  EIF3G  |  DISEASES
10343  |  PKDREJ  |  DISEASES
56135  |  PCDHAC1  |  DISEASES
50617  |  ATP6V0A4  |  DISEASES
6382  |  SDC1  |  DISEASES
1401  |  CRP  |  DISEASES
4608  |  MYBPH  |  DISEASES
759  |  CA1  |  DISEASES
81494  |  CFHR5  |  DISEASES
2694  |  GIF  |  DISEASES
4907  |  NT5E  |  DISEASES
7024  |  TFCP2  |  DISEASES
5279  |  PIGC  |  DISEASES
3569  |  IL6  |  DISEASES
9394  |  HS6ST1  |  DISEASES
2995  |  GYPC  |  DISEASES
84547  |  PGBD1  |  DISEASES
9982  |  FGFBP1  |  DISEASES
7057  |  THBS1  |  DISEASES
9493  |  KIF23  |  DISEASES
64240  |  ABCG5  |  DISEASES
9627  |  SNCAIP  |  DISEASES
7450  |  VWF  |  DISEASES
51274  |  KLF3  |  DISEASES
4124  |  MAN2A1  |  DISEASES
23495  |  TNFRSF13B  |  DISEASES
26035  |  GLCE  |  DISEASES
8482  |  SEMA7A  |  DISEASES
54825  |  CDHR2  |  DISEASES
5939  |  RBMS2  |  DISEASES
64375  |  IKZF4  |  DISEASES
7528  |  YY1  |  DISEASES
945  |  CD33  |  DISEASES
3674  |  ITGA2B  |  DISEASES
6521  |  SLC4A1  |  DISEASES
1459  |  CSNK2A2  |  DISEASES
10483  |  SEC23B  |  DISEASES
3249  |  HPN  |  DISEASES
25939  |  SAMHD1  |  DISEASES
3783  |  KCNN4  |  DISEASES
10552  |  ARPC1A  |  DISEASES
23523  |  CABIN1  |  DISEASES
55686  |  MREG  |  DISEASES
3553  |  IL1B  |  DISEASES
6403  |  SELP  |  DISEASES
55850  |  USE1  |  DISEASES
10664  |  CTCF  |  DISEASES
2817  |  GPC1  |  DISEASES
1371  |  CPOX  |  DISEASES
941  |  CD80  |  DISEASES
119  |  ADD2  |  DISEASES
84162  |  KIAA1109  |  DISEASES
1356  |  CP  |  DISEASES
7067  |  THRA  |  DISEASES
5443  |  POMC  |  DISEASES
118  |  ADD1  |  DISEASES
3383  |  ICAM1  |  DISEASES
10661  |  KLF1  |  DISEASES
7535  |  ZAP70  |  DISEASES
80321  |  CEP70  |  DISEASES
683  |  BST1  |  DISEASES
64083  |  GOLPH3  |  DISEASES
10427  |  SEC24B  |  DISEASES
5576  |  PRKAR2A  |  DISEASES
286  |  ANK1  |  DISEASES
3263  |  HPX  |  DISEASES
51458  |  RHCG  |  DISEASES
8128  |  ST8SIA2  |  DISEASES
1039  |  CDR2  |  DISEASES
9611  |  NCOR1  |  DISEASES
207  |  AKT1  |  DISEASES
5226  |  PGD  |  DISEASES
2212  |  FCGR2A  |  DISEASES
3930  |  LBR  |  DISEASES
5972  |  REN  |  DISEASES
64241  |  ABCG8  |  DISEASES
6233  |  RPS27A  |  DISEASES
55347  |  ABHD10  |  DISEASES
83551  |  TAAR8  |  DISEASES
3439  |  IFNA1  |  DISEASES
710  |  SERPING1  |  DISEASES
51604  |  PIGT  |  DISEASES
5805  |  PTS  |  DISEASES
84539  |  MCHR2  |  DISEASES
6326  |  SCN2A  |  DISEASES
925  |  CD8A  |  DISEASES
8526  |  DGKE  |  DISEASES
9955  |  HS3ST3A1  |  DISEASES
7071  |  KLF10  |  DISEASES
2040  |  STOM  |  DISEASES
27163  |  NAAA  |  DISEASES
135228  |  CD109  |  DISEASES
3815  |  KIT  |  DISEASES
56134  |  PCDHAC2  |  DISEASES
1636  |  ACE  |  DISEASES
115650  |  TNFRSF13C  |  DISEASES
5739  |  PTGIR  |  DISEASES
55585  |  UBE2Q1  |  DISEASES
4634  |  MYL3  |  DISEASES
3101  |  HK3  |  DISEASES
5439  |  POLR2J  |  DISEASES
3046  |  HBE1  |  DISEASES
114757  |  CYGB  |  DISEASES
6777  |  STAT5B  |  DISEASES
51728  |  POLR3K  |  DISEASES
6886  |  TAL1  |  DISEASES
6006  |  RHCE  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
5966  |  REL  |  DISEASES
27306  |  HPGDS  |  DISEASES
213  |  ALB  |  DISEASES
151613  |  TTC14  |  DISEASES
5473  |  PPBP  |  DISEASES
5437  |  POLR2H  |  DISEASES
150159  |  SLC9B1  |  DISEASES
327  |  APEH  |  DISEASES
308  |  ANXA5  |  DISEASES
3673  |  ITGA2  |  DISEASES
6228  |  RPS23  |  DISEASES
167153  |  PAPD4  |  DISEASES
3562  |  IL3  |  DISEASES
1437  |  CSF2  |  DISEASES
717  |  C2  |  DISEASES
338323  |  NLRP14  |  DISEASES
51700  |  CYB5R2  |  DISEASES
117155  |  CATSPER2  |  DISEASES
26585  |  GREM1  |  DISEASES
2038  |  EPB42  |  DISEASES
1398  |  CRK  |  DISEASES
9780  |  PIEZO1  |  DISEASES
55957  |  LIN37  |  DISEASES
7001  |  PRDX2  |  DISEASES
719  |  C3AR1  |  DISEASES
51621  |  KLF13  |  DISEASES
54578  |  UGT1A6  |  DISEASES
43  |  ACHE  |  DISEASES
84640  |  USP38  |  DISEASES
2815  |  GP9  |  DISEASES
929  |  CD14  |  DISEASES
54658  |  UGT1A1  |  DISEASES
64342  |  HS1BP3  |  DISEASES
7399  |  USH2A  |  DISEASES
5232  |  PGK2  |  DISEASES
2244  |  FGB  |  DISEASES
2243  |  FGA  |  DISEASES
10484  |  SEC23A  |  DISEASES
160065  |  PATE1  |  DISEASES
51327  |  AHSP  |  DISEASES
112464  |  PRKCDBP  |  DISEASES
4247  |  MGAT2  |  DISEASES
3354  |  HTR1E  |  DISEASES
695  |  BTK  |  DISEASES
2147  |  F2  |  DISEASES
29984  |  RHOD  |  DISEASES
5897  |  RAG2  |  DISEASES
5340  |  PLG  |  DISEASES
115111  |  SLC26A7  |  DISEASES
947  |  CD34  |  DISEASES
836  |  CASP3  |  DISEASES
358  |  AQP1  |  DISEASES
4778  |  NFE2  |  DISEASES
3642  |  INSM1  |  DISEASES
23  |  ABCF1  |  DISEASES
10657  |  KHDRBS1  |  DISEASES
4179  |  CD46  |  DISEASES
5062  |  PAK2  |  DISEASES
3078  |  CFHR1  |  DISEASES
5187  |  PER1  |  DISEASES
931  |  MS4A1  |  DISEASES
1776  |  DNASE1L3  |  DISEASES
1604  |  CD55  |  DISEASES
53347  |  UBASH3A  |  DISEASES
9377  |  COX5A  |  DISEASES
4684  |  NCAM1  |  DISEASES
6819  |  SULT1C2  |  DISEASES
5315  |  PKM  |  DISEASES
3059  |  HCLS1  |  DISEASES
10938  |  EHD1  |  DISEASES
6888  |  TALDO1  |  DISEASES
283111  |  OR51V1  |  DISEASES
5345  |  SERPINF2  |  DISEASES
6181  |  RPLP2  |  DISEASES
3039  |  HBA1  |  DISEASES
55  |  ACPP  |  DISEASES
10954  |  PDIA5  |  DISEASES
8706  |  B3GALNT1  |  DISEASES
5571  |  PRKAG1  |  DISEASES
5441  |  POLR2L  |  DISEASES
60485  |  SAV1  |  DISEASES
55553  |  SOX6  |  DISEASES
161882  |  ZFPM1  |  DISEASES
4094  |  MAF  |  DISEASES
3047  |  HBG1  |  DISEASES
7485  |  WRB  |  DISEASES
716  |  C1S  |  DISEASES
10456  |  HAX1  |  DISEASES
338324  |  S100A7A  |  DISEASES
6667  |  SP1  |  DISEASES
2811  |  GP1BA  |  DISEASES
842  |  CASP9  |  DISEASES
7490  |  WT1  |  DISEASES
1538  |  CYLC1  |  DISEASES
25834  |  MGAT4C  |  DISEASES
6401  |  SELE  |  DISEASES
6007  |  RHD  |  DISEASES
212  |  ALAS2  |  DISEASES
286410  |  ATP11C  |  DISEASES
23768  |  FLRT2  |  DISEASES
166752  |  FREM3  |  DISEASES
2689  |  GH2  |  DISEASES
7318  |  UBA7  |  DISEASES
91624  |  NEXN  |  DISEASES
3043  |  HBB  |  DISEASES
284361  |  EMC10  |  DISEASES
2152  |  F3  |  DISEASES
2266  |  FGG  |  DISEASES
226  |  ALDOA  |  DISEASES
148738  |  HFE2  |  DISEASES
3932  |  LCK  |  DISEASES
3048  |  HBG2  |  DISEASES
53335  |  BCL11A  |  DISEASES
2885  |  GRB2  |  DISEASES
78989  |  COLEC11  |  DISEASES
445329  |  SULT1A4  |  DISEASES
5329  |  PLAUR  |  DISEASES
5313  |  PKLR  |  DISEASES
966  |  CD59  |  DISEASES
83860  |  TAF3  |  DISEASES
349565  |  NMNAT3  |  DISEASES
6776  |  STAT5A  |  DISEASES
1528  |  CYB5A  |  DISEASES
25870  |  SUMF2  |  DISEASES
921  |  CD5  |  DISEASES
5440  |  POLR2K  |  DISEASES
388228  |  SBK1  |  DISEASES
23463  |  ICMT  |  DISEASES
6818  |  SULT1A3  |  DISEASES
545  |  ATR  |  DISEASES
3005  |  H1F0  |  DISEASES
7975  |  MAFK  |  DISEASES
2035  |  EPB41  |  DISEASES
23764  |  MAFF  |  DISEASES
2624  |  GATA2  |  DISEASES
3767  |  KCNJ11  |  DISEASES
5213  |  PFKM  |  DISEASES
6227  |  RPS21  |  DISEASES
6189  |  RPS3A  |  DISEASES
2534  |  FYN  |  DISEASES
23481  |  PES1  |  DISEASES
204  |  AK2  |  DISEASES
200845  |  KCTD6  |  DISEASES
728  |  C5AR1  |  DISEASES
3792  |  KEL  |  DISEASES
116369  |  SLC26A8  |  DISEASES
1785  |  DNM2  |  DISEASES
3240  |  HP  |  DISEASES
120  |  ADD3  |  DISEASES
146059  |  CDAN1  |  DISEASES
6231  |  RPS26  |  DISEASES
6288  |  SAA1  |  DISEASES
3683  |  ITGAL  |  DISEASES
287  |  ANK2  |  DISEASES
8692  |  HYAL2  |  DISEASES
5079  |  PAX5  |  DISEASES
6714  |  SRC  |  DISEASES
56949  |  XAB2  |  DISEASES
2996  |  GYPE  |  DISEASES
2526  |  FUT4  |  DISEASES
131177  |  FAM3D  |  DISEASES
617  |  BCS1L  |  DISEASES
4151  |  MB  |  DISEASES
7037  |  TFRC  |  DISEASES
6693  |  SPN  |  DISEASES
2157  |  F8  |  DISEASES
4478  |  MSN  |  DISEASES
5599  |  MAPK8  |  DISEASES
4311  |  MME  |  DISEASES
1066  |  CES1  |  DISEASES
2993  |  GYPA  |  DISEASES
9953  |  HS3ST3B1  |  DISEASES
1727  |  CYB5R3  |  DISEASES
4519  |  MT-CYB  |  DISEASES
133308  |  SLC9B2  |  DISEASES
4779  |  NFE2L1  |  DISEASES
10580  |  SORBS1  |  DISEASES
23038  |  WDTC1  |  DISEASES
9898  |  UBAP2L  |  DISEASES
961  |  CD47  |  DISEASES
3664  |  IRF6  |  DISEASES
1378  |  CR1  |  DISEASES
1380  |  CR2  |  DISEASES
8444  |  DYRK3  |  DISEASES
84919  |  PPP1R15B  |  DISEASES
51706  |  CYB5R1  |  DISEASES
5788  |  PTPRC  |  DISEASES
5110  |  PCMT1  |  DISEASES
2165  |  F13B  |  DISEASES
3080  |  CFHR2  |  DISEASES
10877  |  CFHR4  |  DISEASES
10878  |  CFHR3  |  DISEASES
3075  |  CFH  |  DISEASES
10090  |  UST  |  DISEASES
9213  |  XPR1  |  DISEASES
462  |  SERPINC1  |  DISEASES
10767  |  HBS1L  |  DISEASES
2214  |  FCGR3A  |  DISEASES
7391  |  USF1  |  DISEASES
962  |  CD48  |  DISEASES
93183  |  PIGM  |  DISEASES
6708  |  SPTA1  |  DISEASES
922  |  CD5L  |  DISEASES
57127  |  RHBG  |  DISEASES
25912  |  C1orf43  |  DISEASES
26097  |  CHTOP  |  DISEASES
7390  |  UROS  |  DISEASES
54544  |  CRCT1  |  DISEASES
5710  |  PSMD4  |  DISEASES
51177  |  PLEKHO1  |  DISEASES
8349  |  HIST2H2BE  |  DISEASES
2209  |  FCGR1A  |  DISEASES
914  |  CD2  |  DISEASES
965  |  CD58  |  DISEASES
51167  |  CYB5R4  |  DISEASES
6877  |  TAF5  |  DISEASES
9653  |  HS2ST1  |  DISEASES
22802  |  CLCA4  |  DISEASES
9635  |  CLCA2  |  DISEASES
55788  |  LMBRD1  |  DISEASES
959  |  CD40LG  |  DISEASES
6005  |  RHAG  |  DISEASES
953  |  ENTPD1  |  DISEASES
3725  |  JUN  |  DISEASES
732  |  C8B  |  DISEASES
84871  |  AGBL4  |  DISEASES
260293  |  CYP4X1  |  DISEASES
11093  |  ADAMTS13  |  DISEASES
7422  |  VEGFA  |  DISEASES
2889  |  RAPGEF1  |  DISEASES
83549  |  UCK1  |  DISEASES
958  |  CD40  |  DISEASES
5476  |  CTSA  |  DISEASES
5328  |  PLAU  |  DISEASES
310  |  ANXA7  |  DISEASES
27328  |  PCDH11X  |  DISEASES
203  |  AK1  |  DISEASES
5230  |  PGK1  |  DISEASES
84890  |  ADO  |  DISEASES
4153  |  MBL2  |  DISEASES
7099  |  TLR4  |  DISEASES
5592  |  PRKG1  |  DISEASES
2268  |  FGR  |  DISEASES
1043  |  CD52  |  DISEASES
7357  |  UGCG  |  DISEASES
2582  |  GALE  |  DISEASES
54829  |  ASPN  |  DISEASES
6850  |  SYK  |  DISEASES
1192  |  CLIC1  |  DISEASES
58530  |  LY6G6D  |  DISEASES
2017  |  CTTN  |  DISEASES
4524  |  MTHFR  |  DISEASES
2623  |  GATA1  |  DISEASES
7454  |  WAS  |  DISEASES
3105  |  HLA-A  |  DISEASES
7056  |  THBD  |  DISEASES
6461  |  SHB  |  DISEASES
83715  |  ESPN  |  DISEASES
140767  |  NRSN1  |  DISEASES
4868  |  NPHS1  |  DISEASES
347541  |  MAGEB5  |  DISEASES
646480  |  FABP9  |  DISEASES
5251  |  PHEX  |  DISEASES
1906  |  EDN1  |  DISEASES
54790  |  TET2  |  DISEASES
3704  |  ITPA  |  DISEASES
10455  |  ECI2  |  DISEASES
3440  |  IFNA2  |  DISEASES
3045  |  HBD  |  DISEASES
51806  |  CALML5  |  DISEASES
5277  |  PIGA  |  DISEASES
3030  |  HADHA  |  DISEASES
3717  |  JAK2  |  DISEASES
10396  |  ATP8A1  |  DISEASES
6624  |  FSCN1  |  DISEASES
83650  |  SLC35G5  |  DISEASES
10274  |  STAG1  |  DISEASES
94  |  ACVRL1  |  DISEASES
146183  |  OTOA  |  DISEASES
6710  |  SPTB  |  DISEASES
2054  |  STX2  |  DISEASES
5450  |  POU2AF1  |  DISEASES
2539  |  G6PD  |  DISEASES
64174  |  DPEP2  |  DISEASES
3426  |  CFI  |  DISEASES
4891  |  SLC11A2  |  DISEASES
2319  |  FLOT2  |  DISEASES
1198  |  CLK3  |  DISEASES
65010  |  SLC26A6  |  DISEASES
2919  |  CXCL1  |  DISEASES
6387  |  CXCL12  |  DISEASES
11184  |  MAP4K1  |  DISEASES
8131  |  NPRL3  |  DISEASES
23028  |  KDM1A  |  DISEASES
25974  |  MMACHC  |  DISEASES
3098  |  HK1  |  DISEASES
728441  |  GGT2  |  DISEASES
7018  |  TF  |  DISEASES
23029  |  RBM34  |  DISEASES
29072  |  SETD2  |  DISEASES
644150  |  WIPF3  |  DISEASES
7852  |  CXCR4  |  DISEASES
9354  |  UBE4A  |  DISEASES
6744  |  SSFA2  |  DISEASES
404281  |  YY2  |  DISEASES
522  |  ATP5J  |  DISEASES
64711  |  HS3ST6  |  DISEASES
8705  |  B3GALT4  |  DISEASES
26086  |  GPSM1  |  DISEASES
56616  |  DIABLO  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
6304  |  SATB1  |  DISEASES
84529  |  C15orf41  |  DISEASES
9278  |  ZBTB22  |  DISEASES
2821  |  GPI  |  DISEASES
389125  |  MUSTN1  |  DISEASES
3586  |  IL10  |  DISEASES
54475  |  NLE1  |  DISEASES
51686  |  OAZ3  |  DISEASES
721  |  C4B  |  DISEASES
629  |  CFB  |  DISEASES
170506  |  DHX36  |  DISEASES
3077  |  HFE  |  DISEASES
28988  |  DBNL  |  DISEASES
1539  |  CYLC2  |  DISEASES
4700  |  NDUFA6  |  DISEASES
85476  |  GFM1  |  DISEASES
80012  |  PHC3  |  DISEASES
56147  |  PCDHA1  |  DISEASES
1379  |  CR1L  |  DISEASES
51428  |  DDX41  |  DISEASES
27071  |  DAPP1  |  DISEASES
2533  |  FYB  |  DISEASES
2994  |  GYPB  |  DISEASES
222537  |  HS3ST5  |  DISEASES
253970  |  SFTA3  |  DISEASES
4067  |  LYN  |  DISEASES
6188  |  RPS3  |  DISEASES
6230  |  RPS25  |  DISEASES
6207  |  RPS13  |  DISEASES
930  |  CD19  |  DISEASES
3684  |  ITGAM  |  DISEASES
3250  |  HPR  |  DISEASES
8972  |  MGAM  |  DISEASES
4522  |  MTHFD1  |  DISEASES
56342  |  PPAN  |  DISEASES
567  |  B2M  |  DISEASES
7732  |  RNF112  |  DISEASES
6139  |  RPL17  |  DISEASES
7716  |  VEZF1  |  DISEASES
6209  |  RPS15  |  DISEASES
6223  |  RPS19  |  DISEASES
7409  |  VAV1  |  DISEASES
283165  |  KIRREL3-AS3  |  DISEASES
58160  |  NFE4  |  DISEASES
26774  |  SNORD80  |  DISEASES
Locus(Waiting for update.)
Disease ID 329
Disease hemolytic anemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:103)
HP:0001873  |  Low platelet count  |  27
HP:0012115  |  Liver inflammation  |  13
HP:0001981  |  Schistocytosis  |  13
HP:0000083  |  Renal insufficiency  |  9
HP:0200084  |  Giant cell hepatitis  |  8
HP:0001919  |  Acute renal failure  |  8
HP:0000822  |  Hypertension  |  6
HP:0000979  |  Purpura  |  5
HP:0002665  |  Lymphoma  |  5
HP:0002090  |  Pneumonia  |  5
HP:0005550  |  Chronic lymphatic leukemia  |  5
HP:0002092  |  Pulmonary artery hypertension  |  5
HP:0001923  |  Reticulocytosis  |  4
HP:0001903  |  Anemia  |  4
HP:0001909  |  Leukemia  |  4
HP:0002904  |  High blood bilirubin levels  |  3
HP:0001973  |  Autoimmune thrombocytopenia  |  3
HP:0006775  |  Multiple myeloma  |  3
HP:0003641  |  Hemoglobin in urine  |  3
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  3
HP:0005575  |  Hemolytic-uremic syndrome  |  3
HP:0000952  |  Yellow skin  |  3
HP:0012189  |  Hodgkin disease  |  3
HP:0001882  |  Decreased blood leukocyte number  |  3
HP:0012119  |  Methemoglobinemia  |  3
HP:0001744  |  Splenomegaly  |  3
HP:0003256  |  Coagulopathy  |  2
HP:0002910  |  Elevated transaminases  |  2
HP:0004444  |  Spherocytosis  |  2
HP:0010972  |  Anemia of inadequate production  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0100279  |  Ulcerative colitis  |  2
HP:0003002  |  Breast carcinoma  |  2
HP:0001876  |  Low blood cell count  |  2
HP:0001394  |  Hepatic cirrhosis  |  2
HP:0001978  |  Extramedullary hematopoiesis  |  2
HP:0005521  |  Disseminated intravascular coagulation  |  2
HP:0001251  |  Ataxia  |  2
HP:0002633  |  Vasculitis  |  2
HP:0002583  |  Colitis  |  2
HP:0009726  |  Renal neoplasm  |  1
HP:0001945  |  Fever  |  1
HP:0200058  |  Angiosarcoma  |  1
HP:0004787  |  Fulminant hepatitis  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0100843  |  Glioblastoma  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0000836  |  Overactive thyroid  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0001081  |  Gallstones  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0002326  |  TIA  |  1
HP:0100724  |  Hypercoagulability  |  1
HP:0200119  |  Acute liver inflammation  |  1
HP:0006859  |  Posterior leukoencephalopathy  |  1
HP:0001927  |  Acanthocytosis  |  1
HP:0002196  |  Myelopathy  |  1
HP:0100584  |  Endocarditis  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0001733  |  Pancreatic inflammation  |  1
HP:0100502  |  Vitamin B12 deficiency  |  1
HP:0001433  |  Enlarged liver and spleen  |  1
HP:0003613  |  Antiphospholipid antibodies  |  1
HP:0005547  |  Myeloproliferative disorder  |  1
HP:0002608  |  Celiac disease  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0030151  |  Cholangitis  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0002094  |  Dyspnea  |  1
HP:0001875  |  Neutropenia  |  1
HP:0100033  |  Tic disorder  |  1
HP:0001287  |  Meningitis  |  1
HP:0000656  |  Ectropion  |  1
HP:0001971  |  Hypersplenism  |  1
HP:0006579  |  Neonatal jaundice  |  1
HP:0000421  |  Bloody nose  |  1
HP:0012410  |  Pure red cell aplasia  |  1
HP:0001643  |  Persistent ductus arteriosus  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0002908  |  Conjugated hyperbilirubinemia  |  1
HP:0002014  |  Diarrhea  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0002148  |  Hypophosphataemia  |  1
HP:0430007  |  Symblepharon  |  1
HP:0002664  |  Neoplasia  |  1
HP:0100522  |  Thymoma  |  1
HP:0000965  |  Livedo reticularis  |  1
HP:0008682  |  Renal tubular necrosis  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0002352  |  Leukoencephalopathy  |  1
HP:0100523  |  Hepatic abscess  |  1
HP:0200059  |  Metastatic angiosarcoma  |  1
HP:0001735  |  Acute pancreatitis  |  1
HP:0012531  |  Pain  |  1
HP:0012174  |  Glioblastoma multiforme  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
Disease ID 329
Disease hemolytic anemia
Manually Symptom
UMLS  | Name(Total Manually Symptoms:37)
C2697310  |  sarcoidosis
C2613439  |  extramedullary hematopoiesis
C2364133  |  infection
C1963148  |  iron overload
C1963124  |  hemoglobinuria
C1801950  |  g syndrome
C1280080  |  posterior mediastinum
C0948600  |  organ failure
C0947622  |  gallstones
C0878544  |  myocardiopathies
C0878544  |  cardiomyopathy
C0877221  |  erythroblastopenia
C0752303  |  urological manifestations
C0746604  |  mitral valve endocarditis
C0553720  |  spherocytosis
C0521530  |  pulmonary consolidation
C0409974  |  lupus erythematosus
C0398564  |  adenylate kinase deficiency
C0398563  |  hexokinase deficiency
C0264490  |  acute respiratory failure
C0235574  |  intravascular hemolysis
C0151773  |  bone marrow hypoplasia
C0079772  |  t cell lymphoma
C0040188  |  tic disorder
C0040053  |  thrombosis
C0034902  |  pure red cell aplasia
C0032453  |  relapsing polychondritis
C0032302  |  mycoplasma pneumoniae pneumonia
C0032285  |  pneumoniae
C0030472  |  paraneoplastic syndrome
C0026848  |  myopathy
C0026654  |  moyamoya syndrome
C0023470  |  myelogenous leukemia
C0022660  |  acute renal failure
C0017920  |  glucose-6-phosphate dehydrogenase deficiency
C0008312  |  primary biliary cirrhosis
C0002874  |  erythroid aplasia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:15)
C0009450  |  infection  |  7
C0017920  |  glucose-6-phosphate dehydrogenase deficiency  |  7
C0019048  |  hemoglobinuria  |  3
C0022660  |  acute renal failure  |  3
C0032285  |  pneumoniae  |  3
C0235574  |  intravascular hemolysis  |  2
C0553720  |  spherocytosis  |  2
C0018952  |  extramedullary hematopoiesis  |  2
C0752303  |  urological manifestations  |  1
C0034902  |  pure red cell aplasia  |  1
C0040188  |  tic disorder  |  1
C0948600  |  organ failure  |  1
C0008350  |  gallstones  |  1
C0409974  |  lupus erythematosus  |  1
C0040053  |  thrombosis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:9)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1127354260309723704ITPAumls:C0002878BeFreeSignificant association of ITPA gene rs1127354 with protection against RB V-induced hemolytic anemia was found in Ukrainian patients with CHC infection.0.1271770412015ITPA203213196CA,G,T
rs121912751221266436521SLC4A1umls:C0002878BeFreedRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.0.126805912012SLC4A11744251241GT
rs1800562158650843077HFEumls:C0002878BeFreeHeterozygosityfor the C282Y mutation in HFE contributes to iron accumulation and fibrosis progression in chronic hepatitis C. Ribavirin could cause dose-dependent reversible haemolytic anaemia, which can be managed with dose reductions or with administration of epoetin alpha at 40,000 IU once weekly without sacrificing the optimal dosing of ribavarin.0.0008143262005HFE626092913GA
rs180056297530423077HFEumls:C0002878BeFreeWe performed PCR-based analysis for the haemochromatosis-related HFE C282Y mutation in an extended family with inherited haemolytic anaemia in which several members exhibited iron overload.0.0008143261998HFE626092913GA
rs1800562193802923077HFEumls:C0002878BeFreeThis report discusses the pathophysiology of iron accumulation in patients with hemolytic anemia combined with HFE C282Y homozygosity.0.0008143262009HFE626092913GA
rs33924146NA3043HBBumls:C0002878CLINVARNA0.121628651NAHBB115226765AG,C
rs371489738221399792539G6PDumls:C0002878BeFreeIn addition, seven new mutations were found: three presented with acute hemolytic anemia following oxidative stress [G6PD Nice (c.1380G>C, p.Glu460Asp), G6PD Roubaix (c.811G>C, p.Val271Leu), and G6PD Toledo (c.496C>T, p.Arg166Cys)], three with different degrees of chronic hemolytic anemia [G6PD Lille (c.821A>T, p.Glu274Val), G6PD Villeurbanne (c.1000_1002delACC, p.Thr334del), and G6PD Amiens (c.1367A>T, p.Asp456Val)] and one found fortuitously G6PD Montpellier (c.1132G>A, p.Gly378Ser).0.1449265022012G6PDX154532722CT
rs386545618119167492539G6PDumls:C0002878BeFreeSome examples include the alanine-to-valine substitution at codon 222 (Ala222-->Val) [DNA: C-to-T substitution at nucleo-tide 677 (677C-->T)] in methylenetetrahydrofolate reductase (NADPH) and the cofactor FAD (in relation to cardiovascular disease, migraines, and rages), the Pro187-->Ser (DNA: 609C-->T) mutation in NAD(P):quinone oxidoreductase 1 [NAD(P)H dehy-drogenase (quinone)] and FAD (in relation to cancer), the Ala44-->Gly (DNA: 131C-->G) mutation in glucose-6-phosphate 1-dehydrogenase and NADP (in relation to favism and hemolytic anemia), and the Glu487-->Lys mutation (present in one-half of Asians) in aldehyde dehydrogenase (NAD + ) and NAD (in relation to alcohol intolerance, Alzheimer disease, and cancer).0.1449265022002NANANANANA
rs386545618119167494524MTHFRumls:C0002878BeFreeSome examples include the alanine-to-valine substitution at codon 222 (Ala222-->Val) [DNA: C-to-T substitution at nucleo-tide 677 (677C-->T)] in methylenetetrahydrofolate reductase (NADPH) and the cofactor FAD (in relation to cardiovascular disease, migraines, and rages), the Pro187-->Ser (DNA: 609C-->T) mutation in NAD(P):quinone oxidoreductase 1 [NAD(P)H dehy-drogenase (quinone)] and FAD (in relation to cancer), the Ala44-->Gly (DNA: 131C-->G) mutation in glucose-6-phosphate 1-dehydrogenase and NADP (in relation to favism and hemolytic anemia), and the Glu487-->Lys mutation (present in one-half of Asians) in aldehyde dehydrogenase (NAD + ) and NAD (in relation to alcohol intolerance, Alzheimer disease, and cancer).0.0005428842002NANANANANA
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:60)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0002878acetaminophenD000082103-90-2anemia, hemolyticMESH:D000743marker/mechanism2716023
C0002878aminosalicylic acidD01013165-49-6anemia, hemolyticMESH:D000743marker/mechanism5058584
C0002878ampicillinD00066769-53-4anemia, hemolyticMESH:D000743marker/mechanism4124995
C0002878bleomycinD00176111056-06-7anemia, hemolyticMESH:D000743marker/mechanism9572663
C0002878bortezomibD000069286-anemia, hemolyticMESH:D000743marker/mechanism16832816
C0002878carbamazepineD002220298-46-4anemia, hemolyticMESH:D000743marker/mechanism18055338
C0002878carbenicillinD0022284697-36-3anemia, hemolyticMESH:D000743marker/mechanism4124995
C0002878carbidopaD00223038821-49-7anemia, hemolyticMESH:D000743marker/mechanism466061
C0002878cefotaximeD00243963527-52-6anemia, hemolyticMESH:D000743marker/mechanism2316002
C0002878ceftazidimeD00244278439-06-2anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878chlorambucilD002699305-03-3anemia, hemolyticMESH:D000743marker/mechanism2816917
C0002878cladribineD0173384291-63-8anemia, hemolyticMESH:D000743marker/mechanism16398735
C0002878chloroquineD0027381954/5/7anemia, hemolyticMESH:D000743marker/mechanism4794122
C0002878chlorpromazineD00274650-53-3anemia, hemolyticMESH:D000743marker/mechanism3925683
C0002878cimetidineD00292751481-61-9anemia, hemolyticMESH:D000743marker/mechanism19874564
C0002878ciprofloxacinD00293985721-33-1anemia, hemolyticMESH:D000743marker/mechanism12911170
C0002878clofazimineD0029912030-63-9anemia, hemolyticMESH:D000743marker/mechanism19274991
C0002878cyclophosphamideD00352050-18-0anemia, hemolyticMESH:D000743marker/mechanism6027686
C0002878cyclosporineD01657259865-13-3anemia, hemolyticMESH:D000743marker/mechanism1611201
C0002878dapsoneD00362280-08-0anemia, hemolyticMESH:D000743marker/mechanism10028001
C0002878cisplatinD00294515663-27-1anemia, hemolyticMESH:D000743marker/mechanism7706473
C0002878diclofenacD00400815307-86-5anemia, hemolyticMESH:D000743marker/mechanism11051389
C0002878diethylstilbestrolD00405456-53-1anemia, hemolyticMESH:D000743marker/mechanism2712071
C0002878digoxinD00407720830-75-5anemia, hemolyticMESH:D000743marker/mechanism4124995
C0002878epirubicinD01525156420-45-2anemia, hemolyticMESH:D000743marker/mechanism9572663
C0002878ethambutolD00497774-55-5anemia, hemolyticMESH:D000743marker/mechanism188103
C0002878fenfluramineD005277458-24-2anemia, hemolyticMESH:D000743marker/mechanism4706826
C0002878fluorouracilD00547251-21-8anemia, hemolyticMESH:D000743marker/mechanism3093413
C0002878folic acidD00549259-30-3anemia, hemolyticMESH:D000743therapeutic5774135
C0002878gemcitabineC056507103882-84-4anemia, hemolyticMESH:D000743marker/mechanism18427761
C0002878hydroxyureaD006918127-07-1anemia, hemolyticMESH:D000743marker/mechanism15558807
C0002878indinavirD019469150378-17-9anemia, hemolyticMESH:D000743marker/mechanism10533645
C0002878indomethacinD00721353-86-1anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878lansoprazoleD064747-anemia, hemolyticMESH:D000743marker/mechanism8997127
C0002878lovastatinD00814875330-75-5anemia, hemolyticMESH:D000743marker/mechanism7653497
C0002878metforminD008687657-24-9anemia, hemolyticMESH:D000743marker/mechanism10644400
C0002878methotrexateD0087271959/5/2anemia, hemolyticMESH:D000743marker/mechanism6871106
C0002878methysergideD008784361-37-5anemia, hemolyticMESH:D000743marker/mechanism5467905
C0002878mitomycinD0166851950/7/7anemia, hemolyticMESH:D000743marker/mechanism1782316
C0002878nabumetoneC03560542924-53-8anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878omeprazoleD00985373590-58-6anemia, hemolyticMESH:D000743marker/mechanism1992636
C0002878oxaliplatinC030110-anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878peginterferon alfa-2bC417083-anemia, hemolyticMESH:D000743marker/mechanism16340643
C0002878phenytoinD01067257-41-0anemia, hemolyticMESH:D000743marker/mechanism1147459
C0002878piperacillinD01087861477-96-1anemia, hemolyticMESH:D000743marker/mechanism10223610
C0002878piroxicamD01089436322-90-4anemia, hemolyticMESH:D000743marker/mechanism3227521
C0002878propylthiouracilD01144151-52-5anemia, hemolyticMESH:D000743marker/mechanism1110434
C0002878pyrimethamineD01173958-14-0anemia, hemolyticMESH:D000743marker/mechanism1124444
C0002878quinineD011803130-95-0anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878ribavirinD01225436791-04-5anemia, hemolyticMESH:D000743marker/mechanism10733558
C0002878rifampinD01229313292-46-1anemia, hemolyticMESH:D000743marker/mechanism11798598
C0002878succimerD004113304-55-2anemia, hemolyticMESH:D000743marker/mechanism7932916
C0002878sulindacD01346738194-50-2anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878tacrolimusD016559109581-93-3anemia, hemolyticMESH:D000743marker/mechanism10743694
C0002878tolmetinD01404626171-23-3anemia, hemolyticMESH:D000743marker/mechanism17381629
C0002878trimethoprimD014295738-70-5anemia, hemolyticMESH:D000743marker/mechanism20589632
C0002878valproic acidD01463599-66-1anemia, hemolyticMESH:D000743marker/mechanism9855327
C0002878vitamin aD01480111103-57-4anemia, hemolyticMESH:D000743marker/mechanism4684742
C0002878vitamin eD0148101406-18-4anemia, hemolyticMESH:D000743marker/mechanism5094252
C0002878vitamin eD0148101406-18-4anemia, hemolyticMESH:D000743therapeutic968551
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)