ORPHA:104010
Intestinal polyposis syndrome
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Intestinal polyposis syndrome | |
| fr | Syndrome de polypose intestinale | |
| de | Intestinales Polyposis-Syndrom | |
| es | Síndrome de poliposis intestinal | |
| it | Sindrome da poliposi intestinale | |
| nl | Intestinale polyposis-syndroom | |
| pt | Polipose intestinal | |
| pl | Zespół polipowatości jelit | |
| cs | Syndrom intestinální polypózy | |
| uk | Синдром поліпозу кишечника | |
| zh | 肠息肉综合征 | |
| tr | Bağırsak polipoz sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015185 | E | validated | |
| MONDO | 15185 | E | validated | |
| MeSH | D044483 | E | validated | |
| UMLS | C0345891 | E | validated | |
| GARD | 19847 | E | validated | |
| MedDRA | 10057018 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:425003Inherited digestive cancer-predisposing syndrome
rare gastroenterological diseases; rare genetic diseases; rare neoplastic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders
Children (15):
- ORPHA:2615845q22 microdeletion syndrome
- ORPHA:401911AXIN2-related polyposis
- ORPHA:220460Attenuated familial adenomatous polyposis
- ORPHA:109Bannayan-Riley-Ruvalcaba syndrome
- ORPHA:201Cowden syndrome
- ORPHA:2930Cronkhite-Canada syndrome
- ORPHA:733Familial adenomatous polyposis
- ORPHA:157794Hereditary mixed polyposis syndrome
- ORPHA:2929Juvenile polyposis syndrome
- ORPHA:480536MSH3-related polyposis
- ORPHA:247798MUTYH-related polyposis
- ORPHA:454840NTHL1-related polyposis
- ORPHA:2869Peutz-Jeghers syndrome
- ORPHA:447877Polymerase proofreading-related polyposis
- ORPHA:157798Serrated polyposis syndrome
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/104010
- This record as JSON: /data/d/104010.json