ORPHA:99818
Turcot syndrome with polyposis
inactive · moved to ORPHA:733Familial adenomatous polyposis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Familial adenomatous polyposis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Turcot syndrome with polyposis | |
| fr | Syndrome de Turcot avec polypose | |
| de | Turcot-Syndrom mit Polyposis | |
| es | Síndrome de Turcot con poliposis | |
| it | Sindrome di Turcot con poliposi | |
| nl | Syndroom van Turcot met polyposis | |
| pt | Síndrome de Turcot com polipose | |
| pl | Zespół Turcota z polipowatością | |
| cs | Turcotův syndrom s polypózou | |
| uk | Синдром Турко з поліпозом | |
| zh | Turcot综合征息肉病型 | |
| tr | Polipoz ile seyreden Turcot sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020497 | E | validated | |
| UMLS | C5681818 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/99818
- This record as JSON: /data/d/99818.json