Ganglioglioma
- Type
- Disease
- Group
- Disorder
- Status
- active
Ganglioglioma is a rare, usually benign, well-circumscribed, often cystic, mixed neuronal-glial tumor (composed of both neoplastic glial and ganglionic elements) which is typically located in the temporal lobe and rarely invades the surrounding tissue. Patients usually present with seizures refractory to medical treatment. Association with neurofibromatosis type I and tuberous sclerosis has been reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ganglioglioma | |
| fr | Gangliogliome | |
| de | Gangliogliom | |
| es | Ganglioglioma | |
| it | Ganglioglioma | |
| nl | Ganglioglioom | |
| pt | Ganglioglioma | |
| pl | Zwojakoglejak | |
| cs | Gangliogliom | |
| uk | Гангліогліома | |
| zh | 神经节神经胶质瘤 | |
| tr | Gangliogliom |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D33.0 | NTBT | attributed | not yet validated |
| ICD-11 | 2A00.21 | NTBT | index | validated |
| MONDO | 0016733 | E | validated | |
| MeSH | D018303 | E | validated | |
| UMLS | C0206716 | E | validated | |
| GARD | 2430 | E | validated | |
| MedDRA | 10017701 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:251934Mixed neuronal-glial tumor
rare neurological diseases; rare neoplastic diseases - ORPHA:101998Rare epilepsy
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/251949
- This record as JSON: /data/d/251949.json