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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   echinococcosis
  

Disease ID 969
Disease echinococcosis
Definition
An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation.
Synonym
cyst hydatid
cyst, hydatid
cysts, hydatid
disease hydatid
echinococciasis
echinococcoses
echinococcosis (disorder)
echinococcosis [disease/finding]
echinococcus disease
echinococcus nos
echinococcus nos (disorder)
hydatid cyst
hydatid cysts
hydatid disease
hydatidoses
hydatidosis
Orphanet
DOID
UMLS
C0013502
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:67)
C0034065  |  pulmonary embolism  |  8
C0001339  |  acute pancreatitis  |  4
C0032326  |  pneumothorax  |  3
C0013502  |  hydatid disease  |  3
C0856761  |  budd-chiari syndrome  |  3
C0013502  |  echinococcosis  |  3
C0013502  |  hydatid cyst  |  3
C0007177  |  pericardial tamponade  |  2
C0151740  |  increased intracranial pressure  |  2
C0030305  |  pancreatitis  |  2
C0020538  |  hypertension  |  2
C0013502  |  hydatid cysts  |  2
C0442874  |  neuropathy  |  1
C0027051  |  myocardial infarct  |  1
C0001175  |  acquired immunodeficiency syndrome  |  1
C0155773  |  portal vein thrombosis  |  1
C0004030  |  aspergillosis  |  1
C0701818  |  choledocholithiasis  |  1
C0004623  |  bacterial infections  |  1
C0032285  |  pneumonia  |  1
C0020541  |  portal hypertension  |  1
C0740457  |  malignant renal tumor  |  1
C0004623  |  bacterial infection  |  1
C0018801  |  heart failure  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0036130  |  salpingitis  |  1
C0037280  |  infestation  |  1
C0041956  |  ureteric obstruction  |  1
C0018801  |  cardiac failure  |  1
C0030486  |  paraplegia  |  1
C0026934  |  mycoplasma  |  1
C0149521  |  recurrent pancreatitis  |  1
C0011334  |  cavities  |  1
C0002170  |  alopecia  |  1
C0019196  |  hepatitis c  |  1
C0031039  |  pericardial effusion  |  1
C0032302  |  mycoplasma pneumoniae pneumonia  |  1
C1956257  |  pulmonary stenosis  |  1
C0031511  |  pheochromocytoma  |  1
C0041316  |  tuberculous lymphadenitis  |  1
C0041296  |  tuberculosis  |  1
C0040053  |  thrombosis  |  1
C0026266  |  mitral regurgitation  |  1
C0014544  |  epilepsy  |  1
C0206633  |  angiomyolipoma  |  1
C0035078  |  renal failure  |  1
C0007177  |  cardiac tamponade  |  1
C0178879  |  obstructive uropathy  |  1
C0042075  |  uropathy  |  1
C0031154  |  peritonitis  |  1
C0022578  |  keratoconus  |  1
C0022661  |  chronic kidney disease  |  1
C0001418  |  adenocarcinoma  |  1
C0158683  |  polycystic liver disease  |  1
C0022354  |  obstructive jaundice  |  1
C0014547  |  focal epilepsy  |  1
C0342199  |  iodine deficiency  |  1
C0013502  |  hydatidosis  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0027726  |  nephrotic syndrome  |  1
C0152018  |  carcinoma of esophagus  |  1
C0019163  |  hepatitis b  |  1
C0032285  |  pneumoniae  |  1
C0022658  |  kidney disease  |  1
C0040963  |  tricuspid stenosis  |  1
C0027051  |  myocardial infarction  |  1
C0019158  |  hepatitis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
213  |  ALB  |  CTD_human
3043  |  HBB  |  CTD_human
7018  |  TF  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:7)
3123  |  HLA-DRB1  |  CIPHER
3127  |  HLA-DRB5  |  CIPHER
6890  |  TAP1  |  CIPHER
6891  |  TAP2  |  CIPHER
213  |  ALB  |  CTD_human
7018  |  TF  |  CTD_human
3043  |  HBB  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:83)
11214  |  AKAP13  |  1.213  |  DISEASES
554  |  AVPR2  |  1.674  |  DISEASES
85316  |  BAGE5  |  1.504  |  DISEASES
153571  |  C5orf38  |  1.425  |  DISEASES
56477  |  CCL28  |  1.435  |  DISEASES
958  |  CD40  |  1.228  |  DISEASES
959  |  CD40LG  |  3.488  |  DISEASES
942  |  CD86  |  2.046  |  DISEASES
1066  |  CES1  |  5.736  |  DISEASES
1380  |  CR2  |  1.109  |  DISEASES
192668  |  CYS1  |  2.873  |  DISEASES
285193  |  DUSP28  |  2.214  |  DISEASES
1910  |  EDNRB  |  1.389  |  DISEASES
1915  |  EEF1A1  |  1.925  |  DISEASES
133584  |  EGFLAM  |  3.118  |  DISEASES
2009  |  EML1  |  2.086  |  DISEASES
2013  |  EMP2  |  1.635  |  DISEASES
57471  |  ERMN  |  3.071  |  DISEASES
132884  |  EVC2  |  1.226  |  DISEASES
2214  |  FCGR3A  |  1.471  |  DISEASES
51303  |  FKBP11  |  2.523  |  DISEASES
2280  |  FKBP1A  |  1.101  |  DISEASES
2281  |  FKBP1B  |  1.384  |  DISEASES
50943  |  FOXP3  |  2.322  |  DISEASES
2625  |  GATA3  |  1.007  |  DISEASES
10767  |  HBS1L  |  2.398  |  DISEASES
8349  |  HIST2H2BE  |  1.542  |  DISEASES
3123  |  HLA-DRB1  |  2.097  |  DISEASES
3239  |  HOXD13  |  1.092  |  DISEASES
338376  |  IFNE  |  2.003  |  DISEASES
3586  |  IL10  |  3.304  |  DISEASES
3605  |  IL17A  |  2.107  |  DISEASES
3767  |  KCNJ11  |  2.354  |  DISEASES
9851  |  KIAA0753  |  1.511  |  DISEASES
4190  |  MDH1  |  3.312  |  DISEASES
4191  |  MDH2  |  1.899  |  DISEASES
4508  |  MT-ATP6  |  3.316  |  DISEASES
4512  |  MT-CO1  |  6.332  |  DISEASES
4519  |  MT-CYB  |  2.376  |  DISEASES
4535  |  MT-ND1  |  6.161  |  DISEASES
4536  |  MT-ND2  |  2.049  |  DISEASES
4537  |  MT-ND3  |  1.324  |  DISEASES
4540  |  MT-ND5  |  1.912  |  DISEASES
4700  |  NDUFA6  |  1.874  |  DISEASES
11188  |  NISCH  |  1.01  |  DISEASES
3164  |  NR4A1  |  1.491  |  DISEASES
2649  |  NR6A1  |  1.375  |  DISEASES
5016  |  OVGP1  |  3.001  |  DISEASES
10957  |  PNRC1  |  2.963  |  DISEASES
55624  |  POMGNT1  |  1.352  |  DISEASES
5499  |  PPP1CA  |  1.564  |  DISEASES
9588  |  PRDX6  |  1.034  |  DISEASES
9791  |  PTDSS1  |  2.308  |  DISEASES
256297  |  PTF1A  |  3.569  |  DISEASES
135250  |  RAET1E  |  1.421  |  DISEASES
6023  |  RMRP  |  1.424  |  DISEASES
6207  |  RPS13  |  1.146  |  DISEASES
6189  |  RPS3A  |  1.567  |  DISEASES
6196  |  RPS6KA2  |  1.093  |  DISEASES
6334  |  SCN8A  |  1.145  |  DISEASES
51100  |  SH3GLB1  |  2.518  |  DISEASES
91137  |  SLC25A46  |  1.444  |  DISEASES
4093  |  SMAD9  |  1.902  |  DISEASES
23583  |  SMUG1  |  2.451  |  DISEASES
26798  |  SNORD51  |  3.656  |  DISEASES
54558  |  SPATA6  |  2.446  |  DISEASES
55576  |  STAB2  |  1.206  |  DISEASES
246329  |  STAC3  |  1.109  |  DISEASES
6815  |  STYX  |  3.762  |  DISEASES
4070  |  TACSTD2  |  1.892  |  DISEASES
7059  |  THBS3  |  3.32  |  DISEASES
117145  |  THEM4  |  1.323  |  DISEASES
387521  |  TMEM189  |  1.287  |  DISEASES
7124  |  TNF  |  2.164  |  DISEASES
8718  |  TNFRSF25  |  1.581  |  DISEASES
27229  |  TUBGCP4  |  1.901  |  DISEASES
114112  |  TXNRD3  |  3.259  |  DISEASES
51366  |  UBR5  |  5.484  |  DISEASES
127933  |  UHMK1  |  3.176  |  DISEASES
11169  |  WDHD1  |  1.665  |  DISEASES
79971  |  WLS  |  1.424  |  DISEASES
22803  |  XRN2  |  2.395  |  DISEASES
81030  |  ZBP1  |  2.46  |  DISEASES
Locus(Waiting for update.)
Disease ID 969
Disease echinococcosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:60)
HP:0002204  |  Pulmonary embolism  |  8
HP:0100845  |  Anaphylactic shock  |  7
HP:0100749  |  Thoracic pain  |  5
HP:0002835  |  Aspiration  |  5
HP:0012531  |  Pain  |  4
HP:0001735  |  Acute pancreatitis  |  4
HP:0000016  |  Urinary retention  |  3
HP:0002639  |  Budd-Chiari syndrome  |  3
HP:0002107  |  Collapsed lung  |  3
HP:0030731  |  Carcinoma  |  2
HP:0002516  |  Intracranial pressure elevation  |  2
HP:0002105  |  Hemoptysis  |  2
HP:0000822  |  Hypertension  |  2
HP:0002664  |  Neoplasia  |  2
HP:0001733  |  Pancreatic inflammation  |  2
HP:0000952  |  Yellow skin  |  2
HP:0001824  |  Weight loss  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0002090  |  Pneumonia  |  1
HP:0030242  |  Blood clot in portal vein  |  1
HP:0100762  |  Hemobilia  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0006706  |  Cystic liver disease  |  1
HP:0003419  |  Low back pain  |  1
HP:0003270  |  Distended abdomen  |  1
HP:0002315  |  Headaches  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0002666  |  Pheochromocytoma  |  1
HP:0001658  |  Myocardial infarction  |  1
HP:0002586  |  Peritonitis  |  1
HP:0002176  |  Spinal cord compression  |  1
HP:0003418  |  Back pain  |  1
HP:0006557  |  Polycystic liver disease  |  1
HP:0100523  |  Hepatic abscess  |  1
HP:0001653  |  Mitral valve insufficiency  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0001596  |  Hair loss  |  1
HP:0002018  |  Nausea  |  1
HP:0002875  |  Exertional dyspnea  |  1
HP:0010446  |  Tricuspid stenosis  |  1
HP:0002017  |  Nausea and vomiting  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0012151  |  Hemothorax  |  1
HP:0001642  |  Pulmonic stenosis  |  1
HP:0100027  |  Recurring pancreatitis  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0000100  |  Nephrosis  |  1
HP:0100681  |  Esophageal duplication  |  1
HP:0012622  |  Chronic kidney disease  |  1
HP:0010550  |  Paraplegia  |  1
HP:0001698  |  Pericardial effusions  |  1
HP:0012532  |  Chronic pain  |  1
HP:0006772  |  Angiomyolipoma  |  1
HP:0002385  |  Paraparesis  |  1
HP:0000563  |  Conical cornea  |  1
HP:0030151  |  Cholangitis  |  1
Disease ID 969
Disease echinococcosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:9)
C2240374  |  eosinophilia
C1611280  |  allergy
C1550639  |  fistula
C1510420  |  cavities
C1384353  |  infestation
C0152025  |  polyneuropathy
C0021308  |  infarction
C0010403  |  cryoglobulinemia
C0007121  |  bronchial carcinoma
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:11)
C0016169  |  fistula  |  9
C0009450  |  infection  |  7
C0034065  |  pulmonary embolism  |  6
C0022354  |  obstructive jaundice  |  2
C0004623  |  bacterial infection  |  2
C0037280  |  infestation  |  1
C0014457  |  eosinophilia  |  1
C0022346  |  jaundice  |  1
C0019079  |  hemoptysis  |  1
C0013922  |  embolism  |  1
C0264558  |  tension pneumothorax  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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 969
Disease echinococcosis
Case(Waiting for update.)