ORPHA:261806
Partial deletion of chromosome 9 syndrome
Synonyms: Partial monosomy of chromosome 9
- 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 | Partial deletion of chromosome 9 syndrome | Partial monosomy of chromosome 9 |
| fr | Syndrome de délétion partielle du chromosome 9 | Monosomie partielle du chromosome 9 |
| de | Chromosom 9-Deletion, partielle | Partielle Monosomie des Chromosoms 9 |
| es | Síndrome de deleción parcial del cromosoma 9 | Monosomía parcial del cromosoma 9 |
| it | Sindrome delezione parziale del cromosoma 9 | Monosomia parziale del cromosoma 9 |
| nl | Partiële deletie van chromosoom 9-syndroom | Partiële monosomie van chromosoom 9 |
| pt | Monossomia parcial do cromossoma 9 | |
| pl | Zespół częściowej delecji chromosomu 9 | Cześciowa monosomia chromosomu 9 |
| cs | Parciální delece chromozomu 9 | Parciální monozomie chromozomu 9 |
| uk | Часткова делеція хромосоми 9 | Часткова моносомія хромосоми 9 |
| zh | 9号染色体部分缺失 | 9号染色体部分单体 |
| tr | 9. kromozomun kısmi delesyonu | 9. kromozomun kısmi monozomisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016874 | E | validated | |
| MONDO | 16874 | E | validated | |
| UMLS | C5679653 | 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:98142Partial autosomal deletion 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/261806
- This record as JSON: /data/d/261806.json