ORPHA:965
Acromegaloid facial appearance syndrome
inactive · moved to ORPHA:1517Cantú syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cantú syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acromegaloid facial appearance syndrome | |
| fr | Syndrome du faciès acromégaloïde | |
| de | Syndrom der akromegalen Gesichtszüge | Akromegaloides Gesichtsbild-Syndrom |
| es | Síndrome de facies acromegaloide | |
| it | Facies acromegaloide | |
| nl | Acromegaloïd aangezichtssyndroom | |
| pt | Síndrome de facies acromegalóide | |
| pl | Zespół akromegaloidalnego wyglądu twarzy | |
| cs | Syndrom akromegaloidně vyhlížejícího obličeje | |
| uk | Синдром акромегалоїдного вигляду обличчя | |
| zh | 肢端肥大样面容综合征 | |
| tr | Akromegaloid yüz görünüm sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 102150 | E | validated | |
| MeSH | C535655 | E | validated | |
| UMLS | C0796280 | E | validated | |
| GARD | 501 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
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/965
- This record as JSON: /data/d/965.json