ORPHA:156207
Macroglossia
- 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 | Macroglossia | |
| fr | Macroglossie | |
| de | Makroglossie | |
| es | Macroglosia | |
| it | Macroglossia | |
| nl | Macroglossie | |
| pt | Macroglossia | |
| pl | Makroglosja | |
| cs | Makroglosie | |
| uk | Макроглосія | |
| zh | 巨舌症 | |
| tr | Makroglossi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q38.2 | E | specific | validated |
| ICD-11 | DA03.5 | E | specific | validated |
| MONDO | 0015496 | E | validated | |
| MONDO | 15496 | E | validated | |
| MeSH | D008260 | E | validated | |
| UMLS | C0024421 | E | validated | |
| GARD | 3342 | E | validated | |
| MedDRA | 10025391 | 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/156207
- This record as JSON: /data/d/156207.json