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Pediatric Disease Annotations & Medicines



   brucellosis
  

Disease ID 226
Disease brucellosis
Definition
Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss.
Synonym
[x]brucellosis, unspecified
[x]brucellosis, unspecified (disorder)
brucelloses
brucellosis (disorder)
brucellosis [disease/finding]
brucellosis due to brucella sp.
brucellosis due to brucella sp. (disorder)
brucellosis due to brucella species
brucellosis due to brucella species (disorder)
brucellosis nos
brucellosis nos (disorder)
brucellosis, nos
brucellosis, unspecified
cyprus fever
cyprus fevers
fever malta
fever mediterranean
fever, cyprus
fever, gibraltar
fever, malta
fever, mediterranean
fever, rock
fever, undulant
fevers, cyprus
fevers, rock
fevers, undulant
gibraltar fever
malta fever
mediterranean fever
melitococcosis
rock fever
rock fevers
undulant fever
undulant fevers
Orphanet
DOID
ICD10
UMLS
C0006309
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:40)
C0014118  |  endocarditis  |  5
C0030312  |  pancytopenia  |  5
C0272412  |  splenic abscess  |  4
C0031046  |  pericarditis  |  3
C0040053  |  thrombosis  |  2
C0270629  |  epidural abscess  |  2
C0041296  |  tuberculosis  |  2
C0040034  |  thrombocytopenia  |  2
C0019158  |  hepatitis  |  2
C0031039  |  pericardial effusion  |  2
C0024291  |  hemophagocytic lymphohistiocytosis  |  2
C0003864  |  arthritis  |  2
C0023895  |  liver disease  |  1
C0013369  |  dysentery  |  1
C0011570  |  depression  |  1
C0021141  |  syndrome of inappropriate secretion of antidiuretic hormone  |  1
C0018378  |  guillain-barre syndrome  |  1
C0949690  |  spondyloarthritis  |  1
C0343084  |  capillary leak syndrome  |  1
C0747256  |  parasitic infection  |  1
C0155765  |  microangiopathy  |  1
C0029443  |  osteomyelitis  |  1
C0036114  |  salmonellosis  |  1
C0031039  |  pericardial effusions  |  1
C0037998  |  splenic infarction  |  1
C0025309  |  meningoencephalitis  |  1
C0038012  |  spondylitis  |  1
C0002871  |  anemia  |  1
C0024205  |  lymphadenitis  |  1
C0032285  |  pneumonia  |  1
C0034150  |  purpura  |  1
C0022660  |  acute renal failure  |  1
C0035078  |  renal failure  |  1
C0025469  |  mesenteric lymphadenitis  |  1
C0042384  |  vasculitis  |  1
C0151436  |  leukocytoclastic vasculitis  |  1
C0039103  |  synovitis  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0015230  |  rash  |  1
C0012624  |  spondylodiscitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:20)
1234  |  CCR5  |  infer
929  |  CD14  |  infer
2212  |  FCGR2A  |  infer
3458  |  IFNG  |  infer
3586  |  IL10  |  infer
3557  |  IL1RN  |  infer
3558  |  IL2  |  infer
3565  |  IL4  |  infer
3569  |  IL6  |  infer
100507436  |  MICA  |  infer
5696  |  PSMB8  |  infer
5698  |  PSMB9  |  infer
6402  |  SELL  |  infer
6556  |  SLC11A1  |  infer
6890  |  TAP1  |  infer
6891  |  TAP2  |  infer
7040  |  TGFB1  |  infer
7099  |  TLR4  |  infer
7124  |  TNF  |  infer
4210  |  MEFV  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:169)
7132  |  TNFRSF1A  |  DISEASES
3002  |  GZMB  |  DISEASES
26499  |  PLEK2  |  DISEASES
79444  |  BIRC7  |  DISEASES
64743  |  WDR13  |  DISEASES
4210  |  MEFV  |  DISEASES
3191  |  HNRNPL  |  DISEASES
1178  |  CLC  |  DISEASES
973  |  CD79A  |  DISEASES
5444  |  PON1  |  DISEASES
5118  |  PCOLCE  |  DISEASES
6347  |  CCL2  |  DISEASES
51056  |  LAP3  |  DISEASES
6372  |  CXCL6  |  DISEASES
3558  |  IL2  |  DISEASES
6484  |  ST3GAL4  |  DISEASES
969  |  CD69  |  DISEASES
4598  |  MVK  |  DISEASES
3458  |  IFNG  |  DISEASES
80329  |  ULBP1  |  DISEASES
55856  |  ACOT13  |  DISEASES
6206  |  RPS12  |  DISEASES
4012  |  LNPEP  |  DISEASES
3565  |  IL4  |  DISEASES
7903  |  ST8SIA4  |  DISEASES
27136  |  MORC1  |  DISEASES
6556  |  SLC11A1  |  DISEASES
3336  |  HSPE1  |  DISEASES
8574  |  AKR7A2  |  DISEASES
6402  |  SELL  |  DISEASES
7130  |  TNFAIP6  |  DISEASES
10888  |  GPR83  |  DISEASES
5266  |  PI3  |  DISEASES
55831  |  EMC3  |  DISEASES
3659  |  IRF1  |  DISEASES
8192  |  CLPP  |  DISEASES
11034  |  DSTN  |  DISEASES
27352  |  SGSM3  |  DISEASES
4189  |  DNAJB9  |  DISEASES
10462  |  CLEC10A  |  DISEASES
1401  |  CRP  |  DISEASES
55333  |  SYNJ2BP  |  DISEASES
129607  |  CMPK2  |  DISEASES
50640  |  PNPLA8  |  DISEASES
9700  |  ESPL1  |  DISEASES
23416  |  KCNH3  |  DISEASES
51455  |  REV1  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
7097  |  TLR2  |  DISEASES
1833  |  EPYC  |  DISEASES
4069  |  LYZ  |  DISEASES
3074  |  HEXB  |  DISEASES
4141  |  MARS  |  DISEASES
5862  |  RAB2A  |  DISEASES
7011  |  TEP1  |  DISEASES
5595  |  MAPK3  |  DISEASES
3553  |  IL1B  |  DISEASES
3791  |  KDR  |  DISEASES
9595  |  CYTIP  |  DISEASES
5443  |  POMC  |  DISEASES
3371  |  TNC  |  DISEASES
57561  |  ARRDC3  |  DISEASES
10058  |  ABCB6  |  DISEASES
7112  |  TMPO  |  DISEASES
53831  |  GPR84  |  DISEASES
4123  |  MAN2C1  |  DISEASES
150094  |  SIK1  |  DISEASES
4841  |  NONO  |  DISEASES
11160  |  ERLIN2  |  DISEASES
6291  |  SAA4  |  DISEASES
3606  |  IL18  |  DISEASES
80224  |  NUBPL  |  DISEASES
23420  |  NOMO1  |  DISEASES
3460  |  IFNGR2  |  DISEASES
4041  |  LRP5  |  DISEASES
151112  |  ZSWIM2  |  DISEASES
84666  |  RETNLB  |  DISEASES
213  |  ALB  |  DISEASES
1437  |  CSF2  |  DISEASES
5896  |  RAG1  |  DISEASES
5479  |  PPIB  |  DISEASES
94274  |  PPP1R14A  |  DISEASES
55630  |  SLC39A4  |  DISEASES
90864  |  SPSB3  |  DISEASES
136  |  ADORA2B  |  DISEASES
7275  |  TUB  |  DISEASES
8436  |  SDPR  |  DISEASES
56246  |  MRAP  |  DISEASES
157570  |  ESCO2  |  DISEASES
4135  |  MAP6  |  DISEASES
435  |  ASL  |  DISEASES
624  |  BDKRB2  |  DISEASES
81793  |  TLR10  |  DISEASES
92369  |  SPSB4  |  DISEASES
835  |  CASP2  |  DISEASES
4281  |  MID1  |  DISEASES
6810  |  STX4  |  DISEASES
637  |  BID  |  DISEASES
91662  |  NLRP12  |  DISEASES
2193  |  FARSA  |  DISEASES
7791  |  ZYX  |  DISEASES
284359  |  IZUMO1  |  DISEASES
23014  |  FBXO21  |  DISEASES
29933  |  GPR132  |  DISEASES
9146  |  HGS  |  DISEASES
63827  |  BCAN  |  DISEASES
942  |  CD86  |  DISEASES
5104  |  SERPINA5  |  DISEASES
3916  |  LAMP1  |  DISEASES
340075  |  ARSI  |  DISEASES
9547  |  CXCL14  |  DISEASES
114548  |  NLRP3  |  DISEASES
3805  |  KIR2DL4  |  DISEASES
6129  |  RPL7  |  DISEASES
3329  |  HSPD1  |  DISEASES
3605  |  IL17A  |  DISEASES
23764  |  MAFF  |  DISEASES
3767  |  KCNJ11  |  DISEASES
6133  |  RPL9  |  DISEASES
5879  |  RAC1  |  DISEASES
6288  |  SAA1  |  DISEASES
1822  |  ATN1  |  DISEASES
10219  |  KLRG1  |  DISEASES
26136  |  TES  |  DISEASES
2013  |  EMP2  |  DISEASES
6337  |  SCNN1A  |  DISEASES
54106  |  TLR9  |  DISEASES
58484  |  NLRC4  |  DISEASES
9851  |  KIAA0753  |  DISEASES
9447  |  AIM2  |  DISEASES
7062  |  TCHH  |  DISEASES
284486  |  THEM5  |  DISEASES
5654  |  HTRA1  |  DISEASES
80222  |  TARS2  |  DISEASES
8804  |  CREG1  |  DISEASES
959  |  CD40LG  |  DISEASES
4318  |  MMP9  |  DISEASES
7417  |  VDAC2  |  DISEASES
7099  |  TLR4  |  DISEASES
100507436  |  MICA  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
2098  |  ESD  |  DISEASES
79625  |  NDNF  |  DISEASES
3559  |  IL2RA  |  DISEASES
551  |  AVP  |  DISEASES
283820  |  NOMO2  |  DISEASES
5888  |  RAD51  |  DISEASES
55576  |  STAB2  |  DISEASES
338442  |  HCAR2  |  DISEASES
114609  |  TIRAP  |  DISEASES
23532  |  PRAME  |  DISEASES
408050  |  NOMO3  |  DISEASES
27247  |  NFU1  |  DISEASES
23066  |  CAND2  |  DISEASES
57448  |  BIRC6  |  DISEASES
4125  |  MAN2B1  |  DISEASES
7124  |  TNF  |  DISEASES
4615  |  MYD88  |  DISEASES
2081  |  ERN1  |  DISEASES
84978  |  FRMD5  |  DISEASES
834  |  CASP1  |  DISEASES
3586  |  IL10  |  DISEASES
8725  |  URI1  |  DISEASES
8284  |  KDM5D  |  DISEASES
56899  |  ANKS1B  |  DISEASES
4065  |  LY75  |  DISEASES
9051  |  PSTPIP1  |  DISEASES
10866  |  HCP5  |  DISEASES
Locus(Waiting for update.)
Disease ID 226
Disease brucellosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:35)
HP:0001945  |  Fever  |  6
HP:0001876  |  Low blood cell count  |  5
HP:0100584  |  Endocarditis  |  4
HP:0001701  |  Pericarditis  |  3
HP:0001873  |  Low platelet count  |  2
HP:0100796  |  Orchitis  |  2
HP:0001698  |  Pericardial effusions  |  2
HP:0030005  |  Capillary leak  |  2
HP:0001824  |  Weight loss  |  2
HP:0012115  |  Liver inflammation  |  2
HP:0001369  |  Arthritis  |  2
HP:0003418  |  Back pain  |  1
HP:0001903  |  Anemia  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0002633  |  Vasculitis  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0002045  |  Abnormally low body temperature  |  1
HP:0001337  |  Tremor  |  1
HP:0010885  |  Aseptic necrosis  |  1
HP:0012531  |  Pain  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0100769  |  Synovitis  |  1
HP:0000716  |  Depression  |  1
HP:0000979  |  Purpura  |  1
HP:0002829  |  Arthralgias  |  1
HP:0030692  |  Brain tumor  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0002625  |  Blood clot in a deep vein  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0200119  |  Acute liver inflammation  |  1
HP:0002754  |  Bone infection  |  1
HP:0002090  |  Pneumonia  |  1
HP:0000083  |  Renal insufficiency  |  1
Disease ID 226
Disease brucellosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:108)
C2717961  |  thrombotic microangiopathy
C2711548  |  infectious process
C2364133  |  infection
C2186532  |  liver disease
C1963211  |  pericarditis
C1963083  |  cholecystitis
C1961102  |  acute lymphoblastic leukemia
C1735378  |  chronic polyarthritis
C1611280  |  allergy
C1546654  |  granuloma
C1546533  |  abscess
C1449646  |  primary peritonitis
C1393529  |  vascular complications
C1366535  |  diabetes insipidus
C1328486  |  calculous cholecystitis
C1320684  |  vertebral abscess
C1136085  |  monoclonal gammopathy
C0878631  |  pathergy
C0877378  |  sacral pain
C0876991  |  hemophagocytosis
C0857305  |  thrombocytopenic purpura
C0796095  |  c syndrome
C0752303  |  urological manifestations
C0751908  |  vestibular neuronitis
C0751463  |  nerve root compression
C0751000  |  anterior cerebral artery aneurysm
C0748159  |  pulmonary involvement
C0745754  |  hepatic granuloma
C0743554  |  recurrent epistaxis
C0598340  |  torsion spasm
C0585186  |  cutaneous hypersensitivity
C0574960  |  sacroiliitis
C0564778  |  obstetrical disorders
C0543697  |  mixed cryoglobulinemia
C0497156  |  lymphadenopathy
C0452221  |  spinal osteomyelitis
C0422833  |  ent symptoms
C0409207  |  hip arthritis
C0376293  |  stigmata
C0281900  |  lumbar spondylitis
C0272412  |  splenic abscess
C0271355  |  abducens paralysis
C0267797  |  acute hepatitis
C0264551  |  exudative pleural effusion
C0264097  |  calcaneal apophysitis
C0240111  |  knee arthritis
C0239161  |  dactylitis
C0235557  |  pulmonary granuloma
C0235369  |  granulomatous hepatitis
C0235169  |  excitability
C0235031  |  neurological symptoms
C0233777  |  hallucinosis
C0231230  |  fatigability
C0221239  |  rapidly progressive glomerulonephritis
C0155288  |  papilledema
C0155223  |  dacryoadenitis
C0151436  |  allergic vasculitis
C0149881  |  epididymoorchitis
C0149881  |  epididymo-orchitis
C0149871  |  deep venous thrombosis
C0085435  |  reactive arthritis
C0085222  |  psoas abscess
C0040053  |  thrombosis
C0040034  |  thrombocytopenia
C0038012  |  spondylitis
C0037285  |  skin manifestations
C0037285  |  skin manifestation
C0037284  |  skin lesions
C0035435  |  rheumatism
C0035304  |  retinal degenerations
C0032587  |  polyradiculoneuropathy
C0032541  |  polyneuritis
C0031154  |  peritonitis
C0031117  |  peripheral neuropathies
C0030486  |  paraplegia
C0030312  |  pancytopenia
C0029400  |  osteitis
C0029191  |  orchitis
C0027765  |  nervous system diseases
C0027121  |  myositis
C0025311  |  meningomyelitis
C0025309  |  meningoencephalitis
C0024291  |  hemophagocytic syndrome
C0024205  |  lymphadenitis
C0023885  |  hepatic abscess
C0023355  |  leptomeningitis
C0022568  |  keratitis
C0021141  |  syndrome of inappropriate secretion of antidiuretic hormone
C0020532  |  hypersplenism
C0019080  |  hemorrhage
C0017658  |  glomerulonephritis
C0015397  |  ocular disease
C0015230  |  exanthem
C0014743  |  erythema nodosum
C0014583  |  episcleritis
C0014118  |  endocarditis
C0014038  |  encephalitis
C0013504  |  hepatic hydatidosis
C0012624  |  spondylodiscitis
C0012624  |  discitis
C0004610  |  bacteremia
C0004610  |  bacteraemia
C0003864  |  arthritis
C0003708  |  arachnoiditis
C0002878  |  hemolytic anemia
C0001621  |  adrenal gland disorders
C0001403  |  addison's disease
C0001339  |  acute pancreatitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:24)
C0009450  |  infection  |  15
C0000833  |  abscess  |  7
C0030312  |  pancytopenia  |  5
C0014118  |  endocarditis  |  4
C0272412  |  splenic abscess  |  4
C0031046  |  pericarditis  |  3
C0029191  |  orchitis  |  2
C0003864  |  arthritis  |  2
C0040034  |  thrombocytopenia  |  2
C0040053  |  thrombosis  |  1
C0796095  |  c syndrome  |  1
C0024205  |  lymphadenitis  |  1
C0037284  |  skin lesions  |  1
C0038012  |  spondylitis  |  1
C0025309  |  meningoencephalitis  |  1
C0004610  |  bacteremia  |  1
C0574960  |  sacroiliitis  |  1
C0012624  |  spondylodiscitis  |  1
C0422833  |  ent symptoms  |  1
C2717961  |  thrombotic microangiopathy  |  1
C0876991  |  hemophagocytosis  |  1
C0023895  |  liver disease  |  1
C0748159  |  pulmonary involvement  |  1
C0267797  |  acute hepatitis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:6)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1131498165856366402SELLumls:C0006309BeFreeAssociation between the Phe206Leu polymorphism of L-selectin and brucellosis.0.0053628242006SELL1169707345AG
rs11466023253188084210MEFVumls:C0006309BeFreeMediterranean fever (MEFV) variant P369S/R408Q in a patient with entero-Behçet's disease who successfully responded to treatment with colchicine.0.0088816372015MEFV163249586GT,A
rs11466024253188084210MEFVumls:C0006309BeFreeMediterranean fever (MEFV) variant P369S/R408Q in a patient with entero-Behçet's disease who successfully responded to treatment with colchicine.0.0088816372015MEFV163249468CT
rs24766011910764126191PTPN22umls:C0006309BeFreePTPN22 C1858T polymorphism and human brucellosis.0.0026384742009PTPN22;AP4B1-AS11113834946AG
rs3743930212102664210MEFVumls:C0006309BeFreeGenetic analysis was done and heterozygous mutation E148Q was detected as a disease-causing Mediterranean fever (MEFV) mutation.0.0088816372011MEFV163254626CG
rs386580517165856366402SELLumls:C0006309BeFreeAssociation between the Phe206Leu polymorphism of L-selectin and brucellosis.0.0053628242006NANANANANA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0006309rifampinD01229313292-46-1brucellosisMESH:D002006therapeutic16236685
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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