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PedAM

Pediatric Disease Annotations & Medicines



   central pontine myelinolysis
  

Disease ID 1566
Disease central pontine myelinolysis
Definition
A demyelinating condition affecting the PONS and characterized clinically by an acute progressive QUADRIPLEGIA; DYSARTHRIA; DYSPHAGIA; and alterations of consciousness. Pathologic features include prominent demyelination in the central PONS with sparing of axons and neurons. This condition is usually associated with systemic disorders such as HYPONATREMIA; chronic ALCOHOLISM; LIVER FAILURE; severe BURNS; malignant NEOPLASMS; hemorrhagic PANCREATITIS; HEMODIALYSIS; and SEPSIS. The rapid medical correction of hyponatremia has been cited as a cause of this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1125-6)
Synonym
central pontine myelinoclasis
central pontine myelinolysis (disorder)
central pontine myelinosis
myelinoclasis, central pontine
myelinolysis, central pontine
myelinolysis, central pontine [disease/finding]
pontine myelinolysis, central
DOID
ICD10
UMLS
C0206083
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:12)
C0206083  |  central pontine myelinolysis  |  16
C0020450  |  hyperemesis gravidarum  |  1
C0235250  |  hyperemesis  |  1
C0079731  |  b-cell lymphoma  |  1
C0376545  |  hematological malignancies  |  1
C0085543  |  epilepsia partialis continua  |  1
C0024299  |  lymphoma  |  1
C0019829  |  hodgkin lymphoma  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0019202  |  wilson disease  |  1
C0079744  |  diffuse large b-cell lymphoma  |  1
C0014544  |  epilepsia  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:21)
6543  |  SLC8A2  |  DISEASES
55640  |  FLVCR2  |  DISEASES
3630  |  INS  |  DISEASES
50617  |  ATP6V0A4  |  DISEASES
23523  |  CABIN1  |  DISEASES
760  |  CA2  |  DISEASES
6529  |  SLC6A1  |  DISEASES
55957  |  LIN37  |  DISEASES
171558  |  PTCRA  |  DISEASES
375611  |  SLC26A5  |  DISEASES
358  |  AQP1  |  DISEASES
2305  |  FOXM1  |  DISEASES
5498  |  PPOX  |  DISEASES
2526  |  FUT4  |  DISEASES
112476  |  PRRT2  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
551  |  AVP  |  DISEASES
4155  |  MBP  |  DISEASES
361  |  AQP4  |  DISEASES
4099  |  MAG  |  DISEASES
5744  |  PTHLH  |  DISEASES
Locus(Waiting for update.)
Disease ID 1566
Disease central pontine myelinolysis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:10)
HP:0001337  |  Tremor  |  2
HP:0011096  |  Demyelination  |  2
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0002665  |  Lymphoma  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0012188  |  Hyperemesis gravidarum  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0012847  |  Epilepsia partialis continua  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0003228  |  High blood sodium levels  |  1
Disease ID 1566
Disease central pontine myelinolysis
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:3)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0206083cyclophosphamideD00352050-18-0myelinolysis, central pontineMESH:D017590marker/mechanism18988633
C0206083methotrexateD0087271959/5/2myelinolysis, central pontineMESH:D017590marker/mechanism17357801
C0206083tacrolimusD016559109581-93-3myelinolysis, central pontineMESH:D017590marker/mechanism12819864
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)