ORPHA:300576
Oligodontia-cancer predisposition syndrome
inactive · moved to ORPHA:401911AXIN2-related polyposis
Synonyms: Autosomal dominant ectodermal dysplasia-cancer predisposition 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 AXIN2-related attenuated familial adenomatous polyposis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Oligodontia-cancer predisposition syndrome | Autosomal dominant ectodermal dysplasia-cancer predisposition syndrome |
| fr | Syndrome de prédisposition au cancer-oligodontie | Syndrome de dysplasie ectodermique autosomique dominante-prédisposition au cancer |
| de | Oligodontie-Krebs-Prädispositionssyndrom | Ektodermales Dysplasie-Krebs-Prädispositionssyndrom, autosomal-dominantes |
| es | Oligodoncia-síndrome de predisposición al cáncer | Displasia ectodérmica autosómica dominante-síndrome de predisposición al cáncer |
| it | Sindrome oligodontia-predisposizione al cancro | Displasia ectodermica autosomica dominante - sindroma da predisposizione al cancro |
| nl | Oligodontie - kankerpredispositie-syndroom | Autosomaal dominante ectodermale dysplasie - kankerpredispositie-syndroom |
| pt | Síndrome de displasia - neoplasia ectodérmica autossómica dominante | |
| pl | Zespół oligodoncja - predyspozycja do nowotworów | Zespół autosomalna dominująca dysplazja ektodermalna - predyspozycja do nowotworów |
| cs | Syndrom zahrnující oligodoncii a predispozici k nádorům | Syndrom zahrnující autozomálně dominantní ektodermální dysplázii a predispozici k nádorům |
| uk | Синдром олігодонтії-схильності до раку | Аутосомно-домінантний синдром схильності до ектодермальної дисплазії та раку |
| zh | 少牙畸形-癌症易感综合征 | 常染色体显性遗传外胚层发育不良-癌症易感性综合征 |
| tr | Oligodonti-kanser yatkınlık sendromu | Otozomal baskın ektodermal displazi-kanser yatkınlık sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0012075 | E | validated | |
| UMLS | C4750788 | 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/300576
- This record as JSON: /data/d/300576.json