Arachnoid cyst
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 4 |
| OrphanetNr: | 2356 |
| OMIM Id: |
182990
207790 |
| ICD-10: |
G93.0 |
| UMLs: |
C0078981 |
| MeSH: |
D016080 |
| MedDRA: |
10049005 |
| Snomed: |
33595009 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal recessive Not applicable [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Central nervous system cystic malformation
-Rare developmental defect during embryogenesis -Rare neurologic disease Genetic nonsyndromic central nervous system malformation -Rare genetic disease Pituitary hormone deficiency from meningeal origin -Rare endocrine disease -Rare genetic disease |
Symptom Information:
|
|
(HPO:0010550) | Paraplegia | 10 / 7739 | ||||
|
|
(HPO:0000925) | Abnormality of the vertebral column | 20 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
|
|
(HPO:0100702) | Arachnoid cyst | 15 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|