ORPHA:263723
Polysomy of X chromosome syndrome
- Type
- Category
- 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 | Polysomy of X chromosome syndrome | |
| fr | Syndrome de polysomie du chromosome x | |
| de | Chromosom X-Polysomie | |
| es | Síndrome de polisomía del cromosoma X | |
| it | Sindrome polisomia del cromosoma X | |
| nl | Polysomie van X chromosoom-syndroom | |
| pt | Polissomia do cromossoma X | |
| pl | Zespół polisomii chromosomu X | |
| cs | Polyzomie chromozomu X | |
| uk | Полісомія Х-хромосоми | |
| zh | X染色体多体 | |
| tr | X kromozomunun polizomisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17002 | E | validated | |
| UMLS | C5680726 | 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 (1):
- ORPHA:263717X chromosome number anomaly with female phenotype syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases
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/263723
- This record as JSON: /data/d/263723.json