ORPHA:2125
Sacral hemangiomas-multiple congenital abnormalities syndrome
inactive · moved to ORPHA:83628LUMBAR syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to LUMBAR syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sacral hemangiomas-multiple congenital abnormalities syndrome | |
| fr | Syndrome d'hémangiomes sacrés-anomalies congénitales multiples | |
| de | Steiß-Hämangiome - multiple kongenitale Fehlbildungen | |
| es | Síndrome de hemangiomas sacros-anomalías congénitas múltiples | |
| it | Emangiomi sacrali - anomalie congenite multiple | |
| nl | Sacrale hemangiomen - meervoudige congenitale afwijkingen-syndroom | |
| pt | Síndrome de hemangiomas sagrados-anomalias congénitas múltiplas | |
| pl | Naczyniaki kości krzyżowej - mnogie wady wrodzone | |
| cs | Syndrom zahrnující sakrální hemangiomy a mnohočetné vrozené abnormality | |
| uk | Синдром крижових гемангіом-множинних вроджених аномалій | |
| zh | 骶血管瘤-多发先天畸形综合征 | |
| tr | Sakral hemanjiyomlar - çoklu doğumsal anormallikler sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C2931443 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/2125
- This record as JSON: /data/d/2125.json