ORPHA:98155
Sex-chromosome anomaly syndrome
Synonyms: Allosome 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sex-chromosome anomaly syndrome | Allosome anomaly |
| fr | Syndrome d'anomalies des gonosomes | Anomalies des chromosomes sexuels |
| de | Gonosomen-Anomalie | Anomalie der Geschlechtschromosomen |
| es | Síndrome de anomalía gonosómica | Anomalías en los cromosomas sexuales |
| it | Sindrome anomalia dei cromosomi sessuali | Anomalia dei cromosomi sessuali |
| nl | Gonosomenanomalie-syndroom | Geslachtschromosomenanomalie |
| pt | Anomalia dos gonossomas | |
| pl | Zespół aberracji chromosomów płciowych | Anomalia chromosmów płci |
| cs | Aberace gonozomů | Aberace pohlavních chromozomů |
| uk | Аномалія статевих хромосом | Аномалія алосом |
| zh | 性染色体异常 | 异染色体异常 |
| tr | Cinsiyet kromozomu anomalisi | Allozom anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020058 | E | validated | |
| MeSH | D012729 | E | validated | |
| UMLS | C0036868 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:68335Rare chromosomal anomaly
rare developmental anomalies during embryogenesis; rare genetic diseases
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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/98155
- This record as JSON: /data/d/98155.json