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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   leptospirosis
  

Disease ID 554
Disease leptospirosis
Definition
Infections with bacteria of the genus LEPTOSPIRA.
Synonym
[x]leptospirosis, unspecified
[x]leptospirosis, unspecified (disorder)
cane cutter's fever
fort bragg fever
harvest fever
infection due to leptospira
infection due to leptospira, nos
japanese autumnal fever
leptospiroses
leptospirosis (disorder)
leptospirosis [disease/finding]
leptospirosis nos
leptospirosis nos (disorder)
leptospirosis, nos
leptospirosis, unspecified
mud fever
queensland fever
red water fever
rice-field worker's disease
spirochaetal jaundice
spirochetal jaundice
stuttgart disease
weil disease
Orphanet
DOID
ICD10
UMLS
C0023364
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:28)
C0035078  |  renal failure  |  7
C0040034  |  thrombocytopenia  |  5
C0022660  |  acute renal failure  |  5
C0027059  |  myocarditis  |  4
C1145670  |  respiratory failure  |  3
C0030305  |  pancreatitis  |  3
C0019101  |  hemorrhagic fever with renal syndrome  |  1
C0031046  |  pericarditis  |  1
C0032285  |  pneumonitis  |  1
C0041466  |  typhoid fever  |  1
C1565489  |  renal insufficiency  |  1
C0034155  |  thrombotic thrombocytopenic purpura  |  1
C0022667  |  papillary necrosis  |  1
C0041466  |  typhoid  |  1
C0155686  |  acute myocarditis  |  1
C0085293  |  hepatitis e  |  1
C0001973  |  alcoholism  |  1
C0042164  |  uveitis  |  1
C0027697  |  nephritis  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0022116  |  ischaemia  |  1
C0001339  |  acute pancreatitis  |  1
C0267841  |  acalculous cholecystitis  |  1
C0019158  |  hepatitis  |  1
C0008325  |  cholecystitis  |  1
C0027707  |  interstitial nephritis  |  1
C0024198  |  lyme disease  |  1
C0001126  |  renal tubular acidosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:3)
3119  |  HLA-DQB1  |  CIPHER
3123  |  HLA-DRB1  |  CIPHER
7124  |  TNF  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:55)
55811  |  ADCY10  |  1.366  |  DISEASES
2334  |  AFF2  |  1.935  |  DISEASES
8852  |  AKAP4  |  1.949  |  DISEASES
27329  |  ANGPTL3  |  1.383  |  DISEASES
10018  |  BCL2L11  |  2.705  |  DISEASES
140707  |  BRI3BP  |  3.811  |  DISEASES
149466  |  C1orf210  |  1.696  |  DISEASES
721  |  C4B  |  3.421  |  DISEASES
959  |  CD40LG  |  6.13  |  DISEASES
1003  |  CDH5  |  1.202  |  DISEASES
9635  |  CLCA2  |  1.35  |  DISEASES
7464  |  CORO2A  |  2.06  |  DISEASES
1431  |  CS  |  1.011  |  DISEASES
51428  |  DDX41  |  1.009  |  DISEASES
29940  |  DSE  |  2.065  |  DISEASES
1837  |  DTNA  |  1.443  |  DISEASES
2021  |  ENDOG  |  1.273  |  DISEASES
2152  |  F3  |  2.525  |  DISEASES
2242  |  FES  |  1.049  |  DISEASES
2266  |  FGG  |  1.445  |  DISEASES
2582  |  GALE  |  1.982  |  DISEASES
2710  |  GK  |  1.528  |  DISEASES
29889  |  GNL2  |  1.143  |  DISEASES
3033  |  HADH  |  1.01  |  DISEASES
3030  |  HADHA  |  2.165  |  DISEASES
54363  |  HAO1  |  1.351  |  DISEASES
3052  |  HCCS  |  1.142  |  DISEASES
55733  |  HHAT  |  1.271  |  DISEASES
3127  |  HLA-DRB5  |  1.589  |  DISEASES
81502  |  HM13  |  1.034  |  DISEASES
3240  |  HP  |  1.044  |  DISEASES
3329  |  HSPD1  |  2.714  |  DISEASES
3586  |  IL10  |  2.904  |  DISEASES
3594  |  IL12RB1  |  1.095  |  DISEASES
4018  |  LPA  |  1.05  |  DISEASES
4050  |  LTB  |  2.504  |  DISEASES
4151  |  MB  |  1.89  |  DISEASES
8972  |  MGAM  |  1.651  |  DISEASES
4615  |  MYD88  |  1.653  |  DISEASES
255743  |  NPNT  |  2.256  |  DISEASES
56980  |  PRDM10  |  1.346  |  DISEASES
23221  |  RHOBTB2  |  1.89  |  DISEASES
6181  |  RPLP2  |  3.046  |  DISEASES
6189  |  RPS3A  |  1.541  |  DISEASES
54938  |  SARS2  |  1.287  |  DISEASES
462  |  SERPINC1  |  1.013  |  DISEASES
6557  |  SLC12A1  |  3.059  |  DISEASES
55576  |  STAB2  |  3.118  |  DISEASES
3925  |  STMN1  |  1.402  |  DISEASES
25870  |  SUMF2  |  3.757  |  DISEASES
7096  |  TLR1  |  1.572  |  DISEASES
7099  |  TLR4  |  3.441  |  DISEASES
7124  |  TNF  |  2.659  |  DISEASES
7709  |  ZBTB17  |  2.056  |  DISEASES
643836  |  ZFP62  |  3.166  |  DISEASES
Locus(Waiting for update.)
Disease ID 554
Disease leptospirosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:29)
HP:0001945  |  Fever  |  9
HP:0001873  |  Low platelet count  |  6
HP:0000083  |  Renal insufficiency  |  6
HP:0001919  |  Acute renal failure  |  5
HP:0012819  |  Myocarditis  |  4
HP:0002878  |  Respiratory failure  |  3
HP:0001733  |  Pancreatic inflammation  |  3
HP:0012115  |  Liver inflammation  |  2
HP:0001399  |  Liver failure  |  2
HP:0006554  |  Acute hepatic failure  |  2
HP:0002385  |  Paraparesis  |  2
HP:0100806  |  Sepsis  |  1
HP:0000123  |  Nephritis  |  1
HP:0002155  |  Increased triglycerides  |  1
HP:0001082  |  Cholecystitis  |  1
HP:0000952  |  Yellow skin  |  1
HP:0002105  |  Hemoptysis  |  1
HP:0002615  |  Low blood pressure  |  1
HP:0012418  |  Low blood oxygen level  |  1
HP:0001947  |  Renal tubular acidosis  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0001735  |  Acute pancreatitis  |  1
HP:0001701  |  Pericarditis  |  1
HP:0001970  |  Interstitial nephritis  |  1
HP:0008341  |  Renal tubular acidosis, type I  |  1
HP:0005110  |  Atrial fibrillation  |  1
HP:0000554  |  Uveitis  |  1
HP:0100520  |  Oliguria  |  1
HP:0001941  |  acidemia  |  1
Disease ID 554
Disease leptospirosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:57)
C2364133  |  infection
C2364118  |  weakness
C2203646  |  jaundice
C2073625  |  pleural effusion
C1963266  |  uveitis
C1963211  |  pericarditis
C1963198  |  pancreatitis
C1963164  |  lymphopenia
C1963154  |  renal failure
C1839611  |  n syndrome
C1565662  |  acute renal insufficiency
C1565489  |  renal insufficiency
C1402315  |  vascular lesions
C1299910  |  keratouveitis
C1145670  |  respiratory failure
C1000483  |  anemia
C0948600  |  organ failure
C0871189  |  psychotic symptoms
C0836924  |  thrombocytosis
C0796095  |  c syndrome
C0752303  |  urological manifestations
C0748159  |  pulmonary involvement
C0542035  |  erythroid hypoplasia
C0341697  |  renal impairment
C0275544  |  congenital infection
C0267842  |  acute acalculous cholecystitis
C0221773  |  hyperamylasemia
C0162557  |  acute liver failure
C0162293  |  papillitis
C0152025  |  polyneuropathy
C0151295  |  mononeuritis multiplex
C0085655  |  polymyositis
C0085593  |  chills
C0042165  |  anterior uveitis
C0040034  |  thrombocytopenia
C0037090  |  respiratory symptoms
C0035222  |  adult respiratory distress syndrome
C0033975  |  psychosis
C0031154  |  peritonitis
C0030312  |  pancytopenia
C0025289  |  meningitis
C0022660  |  acute renal failure
C0022660  |  acute kidney failure
C0022658  |  renal disease
C0022658  |  nephropathy
C0022073  |  iridocyclitis
C0020433  |  hyperbilirubinaemia
C0019087  |  hemorrhagic diathesis
C0019080  |  hemorrhage
C0019061  |  hemolytic uremic syndrome
C0015469  |  facial palsy
C0015469  |  facial nerve palsy
C0012739  |  disseminated intravascular coagulation
C0007773  |  cerebral arteritis
C0007222  |  cardiovascular disorders
C0002878  |  hemolytic anemia
C0001339  |  acute pancreatitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:17)
C0019080  |  hemorrhage  |  10
C0009450  |  infection  |  6
C0040034  |  thrombocytopenia  |  6
C0035078  |  renal failure  |  5
C0748159  |  pulmonary involvement  |  5
C0948600  |  organ failure  |  5
C0022660  |  acute renal failure  |  4
C1145670  |  respiratory failure  |  3
C0030305  |  pancreatitis  |  3
C0162557  |  acute liver failure  |  2
C0031046  |  pericarditis  |  1
C1839611  |  n syndrome  |  1
C0341697  |  renal impairment  |  1
C0001339  |  acute pancreatitis  |  1
C0042164  |  uveitis  |  1
C1565489  |  renal insufficiency  |  1
C0796095  |  c syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs5743618257845607096TLR1umls:C0023364BeFreeAssociation of Toll-like receptor 2 Arg753Gln and Toll-like receptor 1 Ile602Ser single-nucleotide polymorphisms with leptospirosis in an Argentine population.0.0002714422015TLR1438797027CA
rs5743618257845607097TLR2umls:C0023364BeFreeAssociation of Toll-like receptor 2 Arg753Gln and Toll-like receptor 1 Ile602Ser single-nucleotide polymorphisms with leptospirosis in an Argentine population.0.0005428842015TLR1438797027CA
rs5743708257845607096TLR1umls:C0023364BeFreeAssociation of Toll-like receptor 2 Arg753Gln and Toll-like receptor 1 Ile602Ser single-nucleotide polymorphisms with leptospirosis in an Argentine population.0.0002714422015TLR24153705165GA
rs5743708257845607097TLR2umls:C0023364BeFreeAssociation of Toll-like receptor 2 Arg753Gln and Toll-like receptor 1 Ile602Ser single-nucleotide polymorphisms with leptospirosis in an Argentine population.0.0005428842015TLR24153705165GA
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 554
Disease leptospirosis
Case(Waiting for update.)