Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   opsoclonus-myoclonus syndrome
  

Disease ID 876
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:21)
C0027819  |  neuroblastoma  |  3
C0026934  |  mycoplasma  |  2
C0032302  |  mycoplasma pneumonia  |  2
C0032285  |  pneumoniae  |  2
C0393571  |  multiple system atrophy  |  1
C0238301  |  nasopharyngeal carcinoma  |  1
C0019196  |  hepatitis c infection  |  1
C0026709  |  mps vi  |  1
C0684249  |  lung carcinoma  |  1
C0007131  |  non-small cell lung cancer  |  1
C0242379  |  lung cancer  |  1
C0004134  |  ataxia  |  1
C0026780  |  mumps  |  1
C0019196  |  hepatitis c  |  1
C0007131  |  non-small-cell lung carcinoma  |  1
C0014038  |  encephalitis  |  1
C0149925  |  small cell lung cancer  |  1
C0751583  |  west nile encephalitis  |  1
C0019158  |  hepatitis  |  1
C0042769  |  virus infection  |  1
C0206718  |  ganglioneuroblastoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
5443  |  POMC  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 876
Disease opsoclonus-myoclonus syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:11)
HP:0003006  |  Neuroblastoma  |  3
HP:0030731  |  Carcinoma  |  2
HP:0002664  |  Neoplasia  |  2
HP:0002315  |  Headaches  |  1
HP:0010543  |  Opsoclonus  |  1
HP:0030358  |  Non-small cell lung carcinoma  |  1
HP:0001251  |  Ataxia  |  1
HP:0006747  |  Ganglioneuroblastoma  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0002383  |  Encephalitis  |  1
Disease ID 876
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.)
Text Mining Genotype(Total 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.)
Disease ID 876
Disease opsoclonus-myoclonus syndrome
Case(Waiting for update.)