ORPHA:96321
Polyploidy 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 | Polyploidy syndrome | |
| fr | Syndrome de polyploïdie | |
| de | Polyploidie | |
| es | Síndrome de poliploidía | |
| it | Sindrome poliploidia | |
| nl | Polyploïdie-syndroom | |
| pt | Poliploidia | |
| pl | Zespół poliploidii | |
| cs | Polyploidie | |
| uk | Поліплоїдія | |
| zh | 多倍体 | |
| tr | Poliploidi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q92.7 | E | specific | validated |
| ICD-11 | LD42 | E | specific | validated |
| MONDO | 0019934 | E | validated | |
| MeSH | D011123 | E | validated | |
| UMLS | C0032578 | 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:68335Rare chromosomal anomaly
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/96321
- This record as JSON: /data/d/96321.json