ORPHA:563951
Isolated congenital aglossia
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Isolated congenital hypoglossia/aglossia
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated congenital aglossia | |
| fr | Aglossie isolée congénitale | |
| de | Aglossie, isolierte, kongenitale | |
| es | Aglosia congénita aislada | |
| it | Aglossia congenita isolata | |
| nl | Geïsoleerde congenitale aglossie | |
| pt | Aglossia congénita isolada | |
| pl | Izolowany wrodzony brak języka | |
| cs | Izolovaná vrozená aglosie | |
| uk | Ізольована вроджена аглосія | |
| zh | 孤立性先天性无舌 | |
| tr | İzole doğumsal aglossi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q38.3 | NTBT | inclusion | validated |
| ICD-11 | LA31.1 | NTBT | index | validated |
| MONDO | 0035410 | E | validated | |
| UMLS | C0158663 | E | validated | |
| MedDRA | 10001501 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:141152Isolated congenital hypoglossia/aglossia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare surgical maxillo-facial diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/563951
- This record as JSON: /data/d/563951.json