PedAM
Pediatric Disease Annotations & Medicines
| brown syndrome | ||||
| Disease ID | 1401 |
|---|---|
| Disease | brown syndrome |
| Definition | Brown Syndrome is a rare eye disorder characterized by defects in eye movements. This disorder may be present at birth (congenital) or may occur as the result of another underlying disorder (acquired). Muscles control the movements of the eyes. Some of these muscles turn the eyeball up and down, move the eyeball from side to side, or enable the eyeball to rotate slightly in its socket. The superior oblique tendon sheath of the superior oblique muscle surrounds the eyeball. The symptoms of Brown Syndrome are caused by abnormalities of this tendon sheath including shortening, thickening, or inflammation. This results in the inability to move the affected eye upward. - NORD Reference: NORD |
| Synonym | brown tendon sheath syndrome brown's (tendon) sheath syndrome brown's sheath syndrome brown's syndrome brown's tendon sheath syndrome brown's tendon sheath syndrome (disorder) browns syndrome brwns sotss - superior oblique tendon sheath syndrome superior oblique tendon sheath syndrome syndrome, brown's tendon sheath tendon sheath syndrome of brown |
| OMIM | |
| DOID | |
| UMLS | C0155339 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:3) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1401 |
|---|---|
| Disease | brown syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
| Disease ID | 1401 |
|---|---|
| Disease | brown syndrome |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C2029673 | head posture |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
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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| (Waiting for update.) | |
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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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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