ORPHA:98159
Chromosome X structural 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Chromosome X structural anomaly syndrome | |
| fr | Syndrome d'anomalie de structure du chromosome x | |
| de | Chromosom X mit Strukturanomalität | |
| es | Síndrome de anomalía estructural del cromosoma X | |
| it | Sindrome anomalia strutturale del cromosoma X | |
| nl | Chromosoom X structurele anomalie-syndroom | |
| pt | Anomalia estrutural do cromossoma X | |
| pl | Zespół aberracji strukturalnych chromosomu X | |
| cs | Strukturní aberace chromozomu X | |
| uk | Структурна аномалія хромосоми Х | |
| zh | X染色体结构异常 | |
| tr | Kromozom X yapısal anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681501 | 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:98157Sex-chromosome structural anomaly syndrome
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/98159
- This record as JSON: /data/d/98159.json