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Pediatric Disease Annotations & Medicines



   toxoplasmosis
  

Disease ID 268
Disease toxoplasmosis
Definition
The acquired form of infection by Toxoplasma gondii in animals and man.
Synonym
[x]toxoplasmosis, unspecified
[x]toxoplasmosis, unspecified (disorder)
infect toxoplasma gondii
infection by toxoplasma gondii
infection by toxoplasma gondii (disorder)
infection by toxoplasma gondii (disorder) [ambiguous]
infection, toxoplasma gondii
infections, toxoplasma gondii
toxoplasma gondii infect
toxoplasma gondii infection
toxoplasma gondii infections
toxoplasmoses
toxoplasmosis (disorder)
toxoplasmosis [disease/finding]
toxoplasmosis nos
toxoplasmosis nos (disorder)
toxoplasmosis, unspecified
DOID
ICD10
UMLS
C0040558
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:93)
C0042164  |  uveitis  |  7
C0036341  |  schizophrenia  |  6
C0020255  |  hydrocephalus  |  3
C0026975  |  myelitis  |  3
C0001175  |  acquired immunodeficiency syndrome  |  3
C0014038  |  encephalitis  |  3
C0008513  |  retinochoroiditis  |  3
C0001175  |  acquired immune deficiency  |  2
C0042167  |  posterior uveitis  |  2
C0026896  |  myasthenia gravis  |  2
C0040560  |  congenital toxoplasmosis  |  2
C0027765  |  nervous system disease  |  2
C0014059  |  acute disseminated encephalomyelitis  |  2
C0025289  |  meningitis  |  2
C0000786  |  spontaneous abortion  |  2
C0001175  |  acquired immunodeficiency syndrome (aids)  |  2
C0014544  |  epilepsy  |  2
C0014070  |  encephalomyelitis  |  2
C0001175  |  acquired immune deficiency syndrome  |  2
C0038379  |  strabismus  |  1
C0030499  |  parasitic diseases  |  1
C0153633  |  brain cancer  |  1
C0011603  |  dermatitis  |  1
C0001175  |  acquired immune deficiency syndrome (aids)  |  1
C0031036  |  polyarteritis nodosa  |  1
C0242379  |  lung cancer  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0029132  |  optic neuropathy  |  1
C0014556  |  temporal lobe epilepsy  |  1
C0038012  |  spondylitis  |  1
C0376545  |  hematologic malignancies  |  1
C0026848  |  muscular diseases  |  1
C0019196  |  hepatitis c  |  1
C0036220  |  kaposi sarcoma  |  1
C0011615  |  atopic dermatitis  |  1
C0041296  |  tuberculosis  |  1
C0039128  |  syphilis  |  1
C0008513  |  chorioretinitis  |  1
C0024419  |  waldenstrom's macroglobulinemia  |  1
C0008370  |  cholestasis  |  1
C1960469  |  left ventricular noncompaction  |  1
C0016085  |  filariasis  |  1
C0035309  |  retinal disease  |  1
C0017178  |  gastrointestinal disorders  |  1
C0032310  |  viral pneumonitis  |  1
C0032285  |  pneumonia  |  1
C0030312  |  pancytopenia  |  1
C0027868  |  neuromuscular diseases  |  1
C1261473  |  sarcoma  |  1
C0027765  |  nervous system diseases  |  1
C0017178  |  gastrointestinal disorder  |  1
C0011633  |  dermatomyositis  |  1
C0549423  |  obstructive hydrocephalus  |  1
C0025362  |  mental retardation  |  1
C0000786  |  miscarriage  |  1
C0019212  |  hepatorenal syndrome  |  1
C0002874  |  aplastic anemia  |  1
C0027765  |  neurological disorder  |  1
C0027868  |  neuromuscular disease  |  1
C0679466  |  cognitive deficits  |  1
C0032000  |  pituitary adenoma  |  1
C0040561  |  ocular toxoplasmosis  |  1
C0030567  |  parkinson's disease  |  1
C0025958  |  microcephaly  |  1
C0008148  |  chlamydia  |  1
C0442874  |  neuropathy  |  1
C0030499  |  parasitic disease  |  1
C0007107  |  cancer of the larynx  |  1
C0035305  |  retinal detachment  |  1
C0042075  |  urological disorders  |  1
C0747256  |  parasitic infection  |  1
C0025202  |  melanoma  |  1
C0019158  |  hepatitis  |  1
C0038013  |  ankylosing spondylitis  |  1
C0037769  |  west syndrome  |  1
C0015397  |  ocular disease  |  1
C0030305  |  pancreatitis  |  1
C0023418  |  leukaemia  |  1
C0024314  |  lymphoproliferative disease  |  1
C0022661  |  end-stage renal disease  |  1
C0007682  |  central nervous system diseases  |  1
C0022658  |  renal disease  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0021053  |  immunologic disorders  |  1
C0007682  |  central nervous system disease  |  1
C0014130  |  endocrine disorders  |  1
C0035333  |  retinitis  |  1
C0003467  |  anxiety  |  1
C0027765  |  neurological disorders  |  1
C0001430  |  adenoma  |  1
C0040558  |  toxoplasmosis  |  1
C0042384  |  angiitis  |  1
C1263846  |  attention deficit hyperactivity disorder  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:169)
928  |  CD9  |  DISEASES
30009  |  TBX21  |  DISEASES
151887  |  CCDC80  |  DISEASES
25807  |  RHBDD3  |  DISEASES
2137  |  EXTL3  |  DISEASES
973  |  CD79A  |  DISEASES
6348  |  CCL3  |  DISEASES
6347  |  CCL2  |  DISEASES
3558  |  IL2  |  DISEASES
81622  |  UNC93B1  |  DISEASES
3458  |  IFNG  |  DISEASES
2026  |  ENO2  |  DISEASES
3003  |  GZMK  |  DISEASES
3565  |  IL4  |  DISEASES
6500  |  SKP1  |  DISEASES
51692  |  CPSF3  |  DISEASES
6718  |  AKR1D1  |  DISEASES
30833  |  NT5C  |  DISEASES
826  |  CAPNS1  |  DISEASES
92797  |  HELB  |  DISEASES
2678  |  GGT1  |  DISEASES
417  |  ART1  |  DISEASES
47  |  ACLY  |  DISEASES
1401  |  CRP  |  DISEASES
1794  |  DOCK2  |  DISEASES
9662  |  CEP135  |  DISEASES
3569  |  IL6  |  DISEASES
2995  |  GYPC  |  DISEASES
7097  |  TLR2  |  DISEASES
6496  |  SIX3  |  DISEASES
51816  |  CECR1  |  DISEASES
9878  |  TOX4  |  DISEASES
10133  |  OPTN  |  DISEASES
3553  |  IL1B  |  DISEASES
9466  |  IL27RA  |  DISEASES
80725  |  SRCIN1  |  DISEASES
3383  |  ICAM1  |  DISEASES
10923  |  SUB1  |  DISEASES
27125  |  AFF4  |  DISEASES
23395  |  LARS2  |  DISEASES
6636  |  SNRPF  |  DISEASES
3687  |  ITGAX  |  DISEASES
3394  |  IRF8  |  DISEASES
7462  |  LAT2  |  DISEASES
4715  |  NDUFB9  |  DISEASES
55004  |  LAMTOR1  |  DISEASES
3606  |  IL18  |  DISEASES
9453  |  GGPS1  |  DISEASES
132  |  ADK  |  DISEASES
163786  |  SASS6  |  DISEASES
729230  |  CCR2  |  DISEASES
1234  |  CCR5  |  DISEASES
6352  |  CCL5  |  DISEASES
1973  |  EIF4A1  |  DISEASES
55692  |  LUC7L  |  DISEASES
6006  |  RHCE  |  DISEASES
27306  |  HPGDS  |  DISEASES
84283  |  TMEM79  |  DISEASES
213  |  ALB  |  DISEASES
3015  |  H2AFZ  |  DISEASES
51752  |  ERAP1  |  DISEASES
9607  |  CARTPT  |  DISEASES
1437  |  CSF2  |  DISEASES
5224  |  PGAM2  |  DISEASES
84889  |  SLC7A3  |  DISEASES
115825  |  WDFY2  |  DISEASES
6901  |  TAZ  |  DISEASES
201161  |  CENPV  |  DISEASES
5347  |  PLK1  |  DISEASES
3308  |  HSPA4  |  DISEASES
54463  |  FAM134B  |  DISEASES
3627  |  CXCL10  |  DISEASES
4430  |  MYO1B  |  DISEASES
7386  |  UQCRFS1  |  DISEASES
56246  |  MRAP  |  DISEASES
6363  |  CCL19  |  DISEASES
125988  |  C19orf70  |  DISEASES
947  |  CD34  |  DISEASES
7351  |  UCP2  |  DISEASES
57101  |  ANO2  |  DISEASES
2907  |  GRINA  |  DISEASES
5551  |  PRF1  |  DISEASES
6950  |  TCP1  |  DISEASES
58492  |  ZNF77  |  DISEASES
2193  |  FARSA  |  DISEASES
1974  |  EIF4A2  |  DISEASES
7378  |  UPP1  |  DISEASES
10539  |  GLRX3  |  DISEASES
6007  |  RHD  |  DISEASES
1937  |  EEF1G  |  DISEASES
54101  |  RIPK4  |  DISEASES
79621  |  RNASEH2B  |  DISEASES
7189  |  TRAF6  |  DISEASES
23583  |  SMUG1  |  DISEASES
9529  |  BAG5  |  DISEASES
7204  |  TRIO  |  DISEASES
8835  |  SOCS2  |  DISEASES
3006  |  HIST1H1C  |  DISEASES
966  |  CD59  |  DISEASES
28986  |  MAGEH1  |  DISEASES
3605  |  IL17A  |  DISEASES
390259  |  BSX  |  DISEASES
25813  |  SAMM50  |  DISEASES
419  |  ART3  |  DISEASES
2224  |  FDPS  |  DISEASES
10219  |  KLRG1  |  DISEASES
26136  |  TES  |  DISEASES
55010  |  PARPBP  |  DISEASES
54106  |  TLR9  |  DISEASES
4519  |  MT-CYB  |  DISEASES
257202  |  GPX6  |  DISEASES
9760  |  TOX  |  DISEASES
10580  |  SORBS1  |  DISEASES
54617  |  INO80  |  DISEASES
163882  |  CNST  |  DISEASES
383  |  ARG1  |  DISEASES
51175  |  TUBE1  |  DISEASES
6280  |  S100A9  |  DISEASES
8349  |  HIST2H2BE  |  DISEASES
5016  |  OVGP1  |  DISEASES
51750  |  RTEL1  |  DISEASES
2633  |  GBP1  |  DISEASES
959  |  CD40LG  |  DISEASES
680  |  BRS3  |  DISEASES
958  |  CD40  |  DISEASES
51552  |  RAB14  |  DISEASES
7321  |  UBE2D1  |  DISEASES
7099  |  TLR4  |  DISEASES
64061  |  TSPYL2  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
3105  |  HLA-A  |  DISEASES
127262  |  TPRG1L  |  DISEASES
79906  |  MORN1  |  DISEASES
9445  |  ITM2B  |  DISEASES
3704  |  ITPA  |  DISEASES
4267  |  CD99  |  DISEASES
55835  |  CENPJ  |  DISEASES
55576  |  STAB2  |  DISEASES
29994  |  BAZ2B  |  DISEASES
51343  |  FZR1  |  DISEASES
10521  |  DDX17  |  DISEASES
4901  |  NRL  |  DISEASES
3029  |  HAGH  |  DISEASES
3119  |  HLA-DQB1  |  DISEASES
8505  |  PARG  |  DISEASES
23308  |  ICOSLG  |  DISEASES
728441  |  GGT2  |  DISEASES
6295  |  SAG  |  DISEASES
1719  |  DHFR  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
3106  |  HLA-B  |  DISEASES
159371  |  SLC35G1  |  DISEASES
4615  |  MYD88  |  DISEASES
3586  |  IL10  |  DISEASES
135656  |  DPCR1  |  DISEASES
27333  |  GOLIM4  |  DISEASES
5890  |  RAD51B  |  DISEASES
573  |  BAG1  |  DISEASES
10189  |  ALYREF  |  DISEASES
51428  |  DDX41  |  DISEASES
3684  |  ITGAM  |  DISEASES
169355  |  IDO2  |  DISEASES
4065  |  LY75  |  DISEASES
567  |  B2M  |  DISEASES
22861  |  NLRP1  |  DISEASES
2232  |  FDXR  |  DISEASES
246734  |  NPCDR1  |  DISEASES
9303  |  SNORD25  |  DISEASES
Locus(Waiting for update.)
Disease ID 268
Disease toxoplasmosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:52)
HP:0000554  |  Uveitis  |  7
HP:0100753  |  Schizophrenia  |  6
HP:0002716  |  Lymph node hyperplasia  |  5
HP:0002721  |  Immunodeficiency  |  4
HP:0001250  |  Seizures  |  4
HP:0002383  |  Encephalitis  |  3
HP:0012486  |  Inflammation of spinal cord  |  3
HP:0000238  |  Nonsyndromal hydrocephalus  |  3
HP:0012123  |  Posterior uveitis  |  2
HP:0000969  |  Dropsy  |  2
HP:0000708  |  Behavioral problems  |  2
HP:0001287  |  Meningitis  |  2
HP:0003473  |  Fatigable weakness  |  2
HP:0005268  |  Spontaneous abortion  |  2
HP:0100242  |  Sarcoma  |  1
HP:0000486  |  Squint eyes  |  1
HP:0012054  |  Choroidal melanoma  |  1
HP:0030682  |  Left ventricular noncompaction  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0000541  |  Detached retina  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0000739  |  Anxiety  |  1
HP:0002090  |  Pneumonia  |  1
HP:0030049  |  Brain abscess  |  1
HP:0001396  |  Cholestasis  |  1
HP:0001047  |  Atopic dermatitis  |  1
HP:0001249  |  Mental retardation  |  1
HP:0100533  |  Ocular inflammation  |  1
HP:0012424  |  Chorioretinitis  |  1
HP:0001733  |  Pancreatic inflammation  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0002861  |  Melanoma  |  1
HP:0000252  |  Small head circumference  |  1
HP:0011531  |  Hyalitis  |  1
HP:0200056  |  Macular scar  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0004305  |  Involuntary muscle contractions  |  1
HP:0002633  |  Vasculitis  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0011450  |  CNS infection  |  1
HP:0001876  |  Low blood cell count  |  1
HP:0000303  |  Increased size of lower jaw  |  1
HP:0012118  |  Cancer of the larynx  |  1
HP:0001945  |  Fever  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0001141  |  Severe visual impairment  |  1
HP:0000505  |  Poor vision  |  1
HP:0007018  |  Attention deficits  |  1
HP:0004749  |  Atrial flutter  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0001915  |  Aplastic anemia  |  1
Disease ID 268
Disease toxoplasmosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:58)
C2712322  |  tachycardia
C2364133  |  infection
C2242550  |  acute polyradiculoneuritis
C1963266  |  uveitis
C1963229  |  retinal detachment
C1963211  |  pericarditis
C1962971  |  myocarditis
C1840264  |  immune suppression
C1527383  |  morphea
C1510428  |  cerebral abscess
C1412002  |  atypical pneumonia
C1397626  |  fetal hydrocephalus
C1373218  |  immunosuppression
C1270169  |  villitis
C0948714  |  vestibular paralysis
C0948600  |  organ failure
C0936254  |  polyradiculoneuritis
C0936251  |  polyradiculitis
C0854268  |  fetal damage
C0796095  |  c syndrome
C0728936  |  circulatory disorders
C0581883  |  deafness
C0497156  |  lymphadenopathy
C0456909  |  blindness
C0393799  |  miller-fisher syndrome
C0275519  |  subacute infection
C0272293  |  chronic thrombocytopenic purpura
C0265144  |  chronic constrictive pericarditis
C0263666  |  juvenile dermatomyositis
C0235031  |  neurological symptoms
C0206061  |  interstitial pneumonia
C0158944  |  congenital infections
C0155686  |  acute myocarditis
C0085655  |  polymyositis
C0043117  |  autoimmune thrombocytopenic purpura
C0042167  |  posterior uveitis
C0037285  |  skin manifestations
C0035333  |  retinitis
C0033975  |  psychoses
C0032059  |  placentitis
C0029132  |  optic neuropathy
C0028866  |  oculomotor nerve palsies
C0026847  |  spinal amyotrophy
C0025469  |  mesenteric lymphadenitis
C0025309  |  meningoencephalitis
C0024205  |  lymphadenitis
C0023501  |  leukemoid reaction
C0019270  |  herniation
C0018784  |  sensorineural hearing loss
C0015403  |  ocular infection
C0014038  |  encephalitis
C0013418  |  dystocia
C0011633  |  dermatomyositis
C0008513  |  retinochoroiditis
C0008512  |  chorioretinal scars
C0007137  |  squamous cell carcinoma
C0004943  |  behcet's syndrome
C0004936  |  mental disorders
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:13)
C0009450  |  infection  |  28
C0042164  |  uveitis  |  7
C0024228  |  lymphadenopathy  |  5
C0008513  |  retinochoroiditis  |  3
C0014038  |  encephalitis  |  3
C0158944  |  congenital infections  |  3
C0021079  |  immunosuppression  |  3
C0042167  |  posterior uveitis  |  2
C0035305  |  retinal detachment  |  1
C0035333  |  retinitis  |  1
C0029132  |  optic neuropathy  |  1
C0796095  |  c syndrome  |  1
C0011633  |  dermatomyositis  |  1
Manually Genotype(Total Text Mining 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:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002860Squamous cell carcinomaMP:0003331increased hepatocellular carcinoma incidence;HP:0000407Sensorineural hearing impairment
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002860Squamous cell carcinomaMP:0000639abnormal adrenal gland morphology;HP:0002716Lymphadenopathy
Chemical(Total Drugs:7)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0040558atovaquoneD05362694015-53-9toxoplasmosisMESH:D014123therapeutic10447880
C0040558ciprofloxacinD00293985721-33-1toxoplasmosisMESH:D014123therapeutic20186551
C0040558cyclophosphamideD00352050-18-0toxoplasmosisMESH:D014123marker/mechanism5120183
C0040558dapsoneD00362280-08-0toxoplasmosisMESH:D014123therapeutic18602405
C0040558folic acidD00549259-30-3toxoplasmosisMESH:D014123therapeutic8228015
C0040558pyrimethamineD01173958-14-0toxoplasmosisMESH:D014123therapeutic15909603
C0040558sulfadiazineD01341168-35-9toxoplasmosisMESH:D014123therapeutic14650303
FDA approved drug and dosage information(Total Drugs:2)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D014123ciprociprofloxacin400MG/40ML (10MG/ML)INJECTABLE;INJECTIONDiscontinuedNoneYesNo
MESH:D014123ciprociprofloxacin250MG/5MLFOR SUSPENSION;ORALPrescriptionABYesNo
FDA labeling changes(Total Drugs:2)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D01412303/25/2004ciprociprofloxacinComplicated UTI and pyelonephritisIndicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1  17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1  17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectivelyLabelingB---Bayer12/18/2003FALSE'
MESH:D01412303/25/2004ciprociprofloxacinComplicated UTI and pyelonephritisIndicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1  17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1  17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectivelyLabelingB---Bayer12/18/2003FALSE'