ORPHA:156212
Hypoglossia/aglossia
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hypoglossia/aglossia | |
| fr | Hypoglossie/aglossie | |
| de | Hypoglossie/Aglossie | |
| es | Hipoglosia/aglosia | |
| it | Ipoglossia/aglossia | |
| nl | Hypoglossie/aglossie | |
| pt | Hipoglossia/aglossia | |
| pl | Niedorozwój/brak języka | |
| cs | Hypoglosie/aglosie | |
| uk | Гіпоглосія/аглосія | |
| zh | 舌发育不全/无舌 | |
| tr | Hipoglossi / aglossia |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q38.3 | E | specific | validated |
| MONDO | 15497 | E | validated | |
| UMLS | C5680662 | 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 (3):
- ORPHA:183583Genetic head and neck malformation
rare genetic diseases - ORPHA:155832Rare head and neck malformation
rare developmental anomalies during embryogenesis - ORPHA:68329Rare maxillo-facial surgical disease
rare surgical maxillo-facial diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/156212
- This record as JSON: /data/d/156212.json