PedAM
Pediatric Disease Annotations & Medicines
| tolosa-hunt syndrome | ||||
| Disease ID | 1799 |
|---|---|
| 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 C0242287 | neuromyotonia | 1 C0040053 | thrombosis | 1 C0002880 | autoimmune hemolytic anemia | 1 C0152176 | trochlear nerve palsy | 1 C0042769 | virus infection | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:9) |
| Locus | (Waiting for update.) |
| Disease ID | 1799 |
|---|---|
| Disease | tolosa-hunt syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:5) |
| Disease ID | 1799 |
|---|---|
| Disease | tolosa-hunt syndrome |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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GWASdb Snp Trait(Total Genotypes:0) | |
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Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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