Nasal glial heterotopia
Synonyms: Nasal glioma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Nasal glial heterotopia is a rare developmental abnormality presenting usually at birth or in early childhood (rarely in adulthood) as a benign, non-pulsatile mass that can lead to nasal obstruction, deformation of the septum and nasal bone, and respiratory distress if untreated. Nasal glial heterotopias have no communication with the central nervous system; however an associated defect in the cribriform plate is sometimes reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Nasal glial heterotopia | Nasal glioma |
| fr | Hétérotopie gliale nasale | Gliome nasal |
| de | Gliom, nasales | Nasengliom |
| es | Heterotopia glial nasal | Glioma nasal |
| it | Eterotopia gliale nasale | Glioma nasale |
| nl | Nasale gliale heterotopie | Nasaal glioom |
| pt | Glioma nasal | |
| pl | Nosowa heterotopia glejowa | Glejak nosa |
| cs | Nosní gliální heterotopie | Nosní gliom |
| uk | Носова гліальна гетеротопія | Гліома носа |
| zh | 鼻部神经胶质异位 | 鼻胶质瘤 |
| tr | Nazal glial heterotopi | Burun gliomu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q30.8 | NTBT | attributed | validated |
| ICD-11 | LA70.Y | NTBT | index | validated |
| MONDO | 0015392 | E | validated | |
| UMLS | C0266490 | E | validated | |
| GARD | 19949 | 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:156246Nose and cavum anomaly
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases - ORPHA:98061Rare otorhinolaryngologic tumor
rare otorhinolaryngological diseases; rare neoplastic 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/141112
- This record as JSON: /data/d/141112.json