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Pediatric Disease Annotations & Medicines



   wernicke encephalopathy
  

Disease ID 1133
Disease wernicke encephalopathy
Definition
An acute neurological disorder characterized by the triad of ophthalmoplegia, ataxia, and disturbances of mental activity or consciousness. Eye movement abnormalities include nystagmus, external rectus palsies, and reduced conjugate gaze. THIAMINE DEFICIENCY and chronic ALCOHOLISM are associated conditions. Pathologic features include periventricular petechial hemorrhages and neuropil breakdown in the diencephalon and brainstem. Chronic thiamine deficiency may lead to KORSAKOFF SYNDROME. (Adams et al., Principles of Neurology, 6th ed, pp1139-42; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp452-3)
Synonym
beriberi, cerebral
cerebral beriberi
disease wernickes
enceph gayet wernicke
enceph wernicke
enceph wernickes
encephalopathies, wernicke
encephalopathy wernicke's
encephalopathy wernickes
encephalopathy, gayet wernicke
encephalopathy, gayet-wernicke
encephalopathy, wernicke
encephalopathy, wernicke's
encephalopathy, wernickes
gayet wernicke enceph
gayet wernicke encephalopathy
gayet-wernicke encephalopathy
gayet-wernicke syndrome
wernicke
wernicke dis
wernicke disease
wernicke enceph
wernicke encephalopathies
wernicke encephalopathy (disorder)
wernicke encephalopathy [disease/finding]
wernicke encephalopathy syndrome
wernicke polioenceph superior hemorrhagic
wernicke polioencephalitis, superior hemorrhagic
wernicke superior hemorrhagic polioenceph
wernicke superior hemorrhagic polioencephalitis
wernicke syndrome
wernicke's disease
wernicke's disease (disorder)
wernicke's encephalopathy
wernicke's polioencephalitis, superior hemorrhagic
wernicke's superior hemorrhagic polioencephalitis
wernicke's syndrome
wernickes
wernickes dis
wernickes enceph
wernickes encephalopathy
wernickes superior hemorrhagic polioenceph
wernickes syndrome
DOID
ICD10
UMLS
C0043121
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:12)
C0001339  |  acute pancreatitis  |  2
C0024623  |  gastric cancer  |  1
C0162429  |  nutritional deficiency  |  1
C0162429  |  malnutrition  |  1
C0235250  |  hyperemesis  |  1
C0023890  |  liver cirrhosis  |  1
C0020450  |  hyperemesis gravidarum  |  1
C0442874  |  neuropathy  |  1
C0039841  |  thiamine deficiency  |  1
C0029132  |  optic neuropathy  |  1
C0003125  |  anorexia nervosa  |  1
C0349464  |  korsakoff syndrome  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
TKT  |  7086  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:58)
84245  |  MRI1  |  DISEASES
266  |  AMELY  |  DISEASES
7494  |  XBP1  |  DISEASES
3162  |  HMOX1  |  DISEASES
5816  |  PVALB  |  DISEASES
10560  |  SLC19A2  |  DISEASES
80218  |  NAA50  |  DISEASES
968  |  CD68  |  DISEASES
55902  |  ACSS2  |  DISEASES
2670  |  GFAP  |  DISEASES
6538  |  SLC6A11  |  DISEASES
2694  |  GIF  |  DISEASES
80704  |  SLC19A3  |  DISEASES
9739  |  SETD1A  |  DISEASES
443  |  ASPA  |  DISEASES
6855  |  SYP  |  DISEASES
8273  |  SLC10A3  |  DISEASES
492  |  ATP2B3  |  DISEASES
80321  |  CEP70  |  DISEASES
6507  |  SLC1A3  |  DISEASES
6506  |  SLC1A2  |  DISEASES
7082  |  TJP1  |  DISEASES
4846  |  NOS3  |  DISEASES
171558  |  PTCRA  |  DISEASES
375611  |  SLC26A5  |  DISEASES
10815  |  CPLX1  |  DISEASES
2353  |  FOS  |  DISEASES
794  |  CALB2  |  DISEASES
2752  |  GLUL  |  DISEASES
660  |  BMX  |  DISEASES
63951  |  DMRTA1  |  DISEASES
706  |  TSPO  |  DISEASES
5155  |  PDGFB  |  DISEASES
2042  |  EPHA3  |  DISEASES
1641  |  DCX  |  DISEASES
6540  |  SLC6A13  |  DISEASES
4137  |  MAPT  |  DISEASES
3716  |  JAK1  |  DISEASES
100506658  |  OCLN  |  DISEASES
3177  |  SLC29A2  |  DISEASES
10814  |  CPLX2  |  DISEASES
5743  |  PTGS2  |  DISEASES
22926  |  ATF6  |  DISEASES
5654  |  HTRA1  |  DISEASES
9118  |  INA  |  DISEASES
2030  |  SLC29A1  |  DISEASES
4318  |  MMP9  |  DISEASES
1025  |  CDK9  |  DISEASES
1896  |  EDA  |  DISEASES
3717  |  JAK2  |  DISEASES
7436  |  VLDLR  |  DISEASES
5888  |  RAD51  |  DISEASES
361  |  AQP4  |  DISEASES
51520  |  LARS  |  DISEASES
7086  |  TKT  |  DISEASES
100506742  |  CASP12  |  DISEASES
9414  |  TJP2  |  DISEASES
3684  |  ITGAM  |  DISEASES
Locus(Waiting for update.)
Disease ID 1133
Disease wernicke encephalopathy
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:7)
HP:0001735  |  Acute pancreatitis  |  2
HP:0004395  |  Malnutrition  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0001259  |  Coma  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0012188  |  Hyperemesis gravidarum  |  1
Disease ID 1133
Disease wernicke encephalopathy
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
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:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0043121thiamineD01383159-43-8wernicke encephalopathyMESH:D014899therapeutic14644703
C0043121zidovudineD01521530516-87-1wernicke encephalopathyMESH:D014899marker/mechanism2882316
FDA approved drug and dosage information(Total Drugs:6)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D014899retrovirzidovudine100MGCAPSULE;ORALPrescriptionABYesYes
MESH:D014899retrovirzidovudine50MG/5MLSYRUP;ORALPrescriptionAAYesYes
MESH:D014899retrovirzidovudine10MG/MLINJECTABLE;INJECTIONPrescriptionAPYesYes
MESH:D014899retrovirzidovudine200MGTABLET;ORALDiscontinuedNoneNoNo
MESH:D014899zidovudinezidovudine60MGTABLET;ORALDiscontinuedNoneNoNo
MESH:D014899zidovudinezidovudine60MGTABLET;ORALDiscontinuedNoneNoNo
FDA labeling changes(Total Drugs:6)
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:D0148996/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0148996/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0148996/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0148996/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D01489909/19/2008retrovir syrup, capsules and tabletszidovudineUsed in combination with 18 other antiretroviral agents for the treatment of HIV-1 infectionDosing and administration information provided to children 6 weeks to less than 18 years of age Macrocytosis was reported in the majority of pediatric patients receiving Retrovir 180 mg/m2 every 6 hours in open-label studies New dosing regimenLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0148996/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'