ORPHA:966
Hypertrichosis-acromegaloid facial appearance syndrome
inactive · moved to ORPHA:1517Cantú syndrome
Synonyms: HAFF · Hypertrichosis-acromegaloid facial features syndrome · Hypertrichosis-coarse face 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 | Hypertrichosis-acromegaloid facial appearance syndrome | HAFF · Hypertrichosis-acromegaloid facial features syndrome · Hypertrichosis-coarse face syndrome |
| fr | Syndrome d'hypertrichose-faciès acromégaloïde | HAFF |
| de | Syndrom des akromegaloiden Gesichtes mit Hypertrichose | HAFF · Hypertrichose-akromegaloide Gesichtszüge-Syndrom |
| es | Síndrome de hipertricosis-apariencia facial acromegaloide | HAFF · Síndrome de hipertricosis-cara tosca · Síndrome de hipertricosis-rasgos faciales acromegaloides |
| it | Sindrome ipertricosi-facies acromegaloide | HAFF · Sindrome ipertricosi-faccia grossolana · Sindrome ipertricosi-tratti facciali acromegaloidi |
| nl | Hypertrichose - acromegaloïd aangezicht-syndroom | HAFF · Hypertrichose - acromegaloïde gelaatskenmerken-syndroom · Hypertrichose - grof aangezicht-syndroom |
| pt | Síndrome de hipertricose-facies acromegalóide | |
| pl | Zespół hipertrichoza - akromegaloidalny wygląd twarzy | Zespół hipertrichoza - akromegaloidalne cechy twarzy · HAFF · Zespół hipertrichoza - grube rysy twarzy |
| cs | Syndrom zahrnující hypertrichózu a akromegaloidně vyhlížející obličej | HAFF · Syndrom zahrnující hypertrichózu a hrubé faciální rysy · Syndrom zahrnující hypertrichózu a akromegaloidní obličejové rysy |
| uk | Синдром гіпертрихозу-акромегалоїдного вигляду обличчя | HAFF · Синдром гіпертрихозно-акромегалоїдних рис обличчя · Синдром гіпертрихозу - грубе обличчя |
| zh | 多毛-肢端肥大样面容综合征 | 多毛-肢端肥大样面容综合征 |
| tr | Hipertrikoz-akromegaloid yüz görünümü sendromu | HAFF · Hipertrikoz-kaba yüz sendromu · Hipertrikoz-akromegaloid fasiyal özellikler sendromu |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/966
- This record as JSON: /data/d/966.json