ORPHA:141115
Nasal ganglioglioma
- Type
- Disease
- Group
- Disorder
- Age of onset
- Antenatal, Neonatal
- Status
- active
Nasal ganglioglioma is a rare tumor, presenting in newborns, containing both neuronal and astrocytic components and that can be endonasal, extranasal or both. It is usually identified as a nasal mass that may cause feeding difficulties and nasal obstruction.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Nasal ganglioglioma | |
| fr | Gangliogliome nasal | |
| de | Gangliogliom, nasales | |
| es | Ganglioglioma nasal | |
| it | Ganglioglioma nasale | |
| nl | Nasaal ganglioglioom | |
| pt | Ganglioglioma nasal | |
| pl | Zwojak nerwowy nosa | |
| cs | Nazální gangliogliom | |
| uk | Гангліогліома носа | |
| zh | 鼻部神经节胶质瘤 | |
| tr | Nazal ganglioglioma |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q30.8 | NTBT | attributed | validated |
| ICD-11 | 2A00.21 | NTBT | index | validated |
| MONDO | 0015393 | E | validated | |
| UMLS | C5548206 | E | validated | |
| GARD | 19950 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98061Rare otorhinolaryngologic tumor
rare otorhinolaryngological diseases; rare neoplastic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 250 cases | Worldwide | Case(s) | Validated | 18093665[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 18093665[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/141115
- This record as JSON: /data/d/141115.json