ORPHA:171836
Amelogenesis imperfecta-gingival hyperplasia syndrome
inactive · moved to ORPHA:1031Enamel-renal syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Enamel-renal syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Amelogenesis imperfecta-gingival hyperplasia syndrome | |
| fr | Syndrome d'amélogenèse imparfaite-hyperplasie gingivale | |
| de | Amelogenesis imperfecta-Zahnfleischhyperplasie-Syndrom | Amelogenesis imperfecta-Gingivahyperplasie-Syndrom |
| es | Síndrome de amelogénesis imperfecta-hiperplasia gingival | |
| it | Sindrome amelogenesi imperfetta-iperplasia gengivale | |
| nl | Amelogenesis imperfecta - gingivale hyperplasie-syndroom | Amelogenesis imperfecta - tandvleeshyperplasie-syndroom |
| pt | Fibromatose gengival - anomalias dentárias | |
| pl | Zespół wrodzonego niedorozwoju szkliwa i hiperplazji dziąseł | |
| cs | Syndrom zahrnující amelogenesis imperfecta a hyperplázii dásní | |
| uk | Синдром недосконалого амелогенезу - гіперплазія ясен | |
| zh | 釉质发育不全-牙龈增生综合征 | |
| tr | Amelogenezis imperfekta-gingival hiperplazi sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/171836
- This record as JSON: /data/d/171836.json