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Pediatric Disease Annotations & Medicines



   opsoclonus-myoclonus syndrome
  

Disease ID 546
Disease opsoclonus-myoclonus syndrome
Definition
A neurological condition that is characterized by uncontrolled rapid irregular movements of the eye (OPSOCLONUS) and the muscle (MYOCLONUS) causing unsteady, trembling gait. It is also known as dancing eyes-dancing feet syndrome and is often associated with neoplasms, viral infections, or autoimmune disorders involving the nervous system.
Synonym
dancing eyes dancing feet syndrome
dancing eyes, dancing feet syndrome
dancing eyes-dancing feet syndrome
opsoclonus myoclonus ataxia
opsoclonus myoclonus syndrome
opsoclonus-myoclonus syndrome (disorder)
opsoclonus-myoclonus syndrome [disease/finding]
Orphanet
UMLS
C0393626
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:20)
C0032285  |  pneumoniae  |  2
C0032302  |  mycoplasma pneumonia  |  2
C0027819  |  neuroblastoma  |  2
C0026934  |  mycoplasma  |  2
C0238301  |  nasopharyngeal carcinoma  |  1
C0393571  |  multiple system atrophy  |  1
C0019196  |  hepatitis c  |  1
C0007131  |  non-small cell lung cancer  |  1
C0149925  |  small cell lung cancer  |  1
C0026780  |  mumps  |  1
C0014038  |  encephalitis  |  1
C0026709  |  mps vi  |  1
C0042769  |  virus infection  |  1
C0206718  |  ganglioneuroblastoma  |  1
C0007131  |  non-small-cell lung carcinoma  |  1
C0751583  |  west nile encephalitis  |  1
C0019158  |  hepatitis  |  1
C0242379  |  lung cancer  |  1
C0019196  |  hepatitis c infection  |  1
C0684249  |  lung carcinoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
POMC  |  5443  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 546
Disease opsoclonus-myoclonus syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:10)
HP:0030731  |  Carcinoma  |  2
HP:0002664  |  Neoplasia  |  2
HP:0003006  |  Neuroblastoma  |  2
HP:0012115  |  Liver inflammation  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0010543  |  Opsoclonus  |  1
HP:0006747  |  Ganglioneuroblastoma  |  1
HP:0030358  |  Non-small cell lung carcinoma  |  1
HP:0002315  |  Headaches  |  1
HP:0002383  |  Encephalitis  |  1
Disease ID 546
Disease opsoclonus-myoclonus syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C0700095  |  neuroblastoma
C0422833  |  ent symptoms
C0149925  |  small cell lung cancer
C0007134  |  renal cell carcinoma
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0027819  |  neuroblastoma  |  2
C0149925  |  small cell lung cancer  |  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:0005584Renal cell carcinomaMP:0004207increased squamous cell carcinoma incidence;
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0005584Renal cell carcinomaMP:0009625abnormal abdominal lymph node morphology;HP:0003006Neuroblastoma
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)