ORPHA:263746
Y chromosome number anomaly 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 | Y chromosome number anomaly syndrome | |
| fr | Syndrome d'anomalie du nombre de chromosome y | |
| de | Chromosom Y-Anomalie, numerische | |
| es | Síndrome de anomalía numérica del cromosoma Y | |
| it | Sindrome anomalia numerica del cromosoma Y | |
| nl | Numerieke anomalie van Y-chromosoom-syndroom | |
| pt | Anomalia do número de cromossoma Y | |
| pl | Zespół aberracji liczbowej chromosomu Y | |
| cs | Anomálie počtu chromozomů Y | |
| uk | Аномалія кількості Y-хромосоми | |
| zh | Y染色体数目异常 | |
| tr | Y kromozom sayısı anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD52 | E | specific | validated |
| MONDO | 17005 | E | validated | |
| UMLS | C4736189 | 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:98156Sex-chromosome number anomaly 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/263746
- This record as JSON: /data/d/263746.json