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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   tolosa hunt syndrome
  

Disease ID 1977
Disease tolosa hunt syndrome
Definition
An idiopathic syndrome characterized by the formation of granulation tissue in the anterior cavernous sinus or superior orbital fissure, producing a painful ophthalmoplegia. (Adams et al., Principles of Neurology, 6th ed, p271)
Synonym
syndrome tolosa-hunt
tolosa-hunt syndrome
tolosa-hunt syndrome (disorder)
tolosa-hunt syndrome [disease/finding]
Orphanet
DOID
UMLS
C0040381
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:6)
C0002878  |  hemolytic anemia  |  1
C0042769  |  virus infection  |  1
C0152176  |  trochlear nerve palsy  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C0242287  |  neuromyotonia  |  1
C0040053  |  thrombosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:5)
959  |  CD40LG  |  1.527  |  DISEASES
4763  |  NF1  |  1.679  |  DISEASES
114548  |  NLRP3  |  2.171  |  DISEASES
3921  |  RPSA  |  3.613  |  DISEASES
23583  |  SMUG1  |  1.014  |  DISEASES
Locus(Waiting for update.)
Disease ID 1977
Disease tolosa hunt syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:5)
Disease ID 1977
Disease tolosa hunt syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
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 1977
Disease tolosa hunt syndrome
Case(Waiting for update.)