PedAM
Pediatric Disease Annotations & Medicines
| arachnoid cysts | ||||
| Disease ID | 1462 |
|---|---|
| Disease | arachnoid cysts |
| Definition | Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) |
| Synonym | arachnoid cyst arachnoid cyst (disorder) arachnoid cysts [disease/finding] arachnoid diverticula arachnoid diverticulas arachnoidal cyst cyst arachnoid cyst, arachnoid cyst, leptomeningeal cysts, arachnoid cysts, leptomeningeal diverticula, arachnoid diverticulas, arachnoid leptomeningeal cyst leptomeningeal cysts |
| Orphanet | |
| DOID | |
| UMLS | C0078981 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:11) C0020255 | hydrocephalus | 2 C0039144 | syringomyelia | 2 C0151740 | increased intracranial pressure | 1 C0162809 | kallmann syndrome | 1 C0085413 | autosomal dominant polycystic kidney disease | 1 C0022679 | cystic kidney | 1 C0085413 | autosomal dominant polycystic kidney | 1 C0003708 | arachnoiditis | 1 C0041341 | tuberous sclerosis complex | 1 C0392548 | cauda equina syndrome | 1 C0041341 | tuberous sclerosis | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1462 |
|---|---|
| Disease | arachnoid cysts |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:9) HP:0000238 | Nonsyndromal hydrocephalus | 2 HP:0003396 | Syringomyelia | 2 HP:0001140 | Epibulbar dermoid | 1 HP:0002516 | Intracranial pressure elevation | 1 HP:0000505 | Poor vision | 1 HP:0002463 | Language impairment | 1 HP:0002176 | Spinal cord compression | 1 HP:0000113 | Polycystic kidney dysplasia | 1 HP:0000078 | Genital abnormalities | 1 |
| Disease ID | 1462 |
|---|---|
| Disease | arachnoid cysts |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:3) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
All Snps(Total Genotypes:1) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
| rs121912911 | 8728690 | 1278 | COL1A2 | umls:C0078981 | BeFree | Arachnoid cyst and chronic subdural haematoma in a child with osteogenesis imperfecta type III resulting from the substitution of glycine 1006 by alanine in the pro alpha 2(I) chain of type I procollagen. | 0.000271442 | 1996 | COL1A2 | 7 | 94426442 | G | C |
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.) |
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.) | |