ORPHA:68335
Rare chromosomal anomaly
- 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 | Rare chromosomal anomaly | |
| fr | Anomalie chromosomique rare | |
| de | Seltene Chromosomenanomalie | |
| es | Anomalías cromosómicas raras | |
| it | Anomalia cromosomica | |
| nl | Zeldzame chromosomale anomalie | |
| pt | Anomalia cromossómica rara | |
| pl | Zaburzenia chromosomowe | |
| cs | Anomálie chromozomů | |
| uk | Рідкісна хромосомна аномалія | |
| zh | 罕见染色体异常 | |
| tr | Nadir kromozom anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19040 | E | validated | |
| MeSH | D002869 | E | validated | |
| UMLS | C5681313 | 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:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis - ORPHA:98053Rare genetic disease
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/68335
- This record as JSON: /data/d/68335.json