ORPHA:2486
Transverse limb deficiency-hemangioma syndrome
inactive · moved to ORPHA:221061Familial cerebral cavernous malformation
- 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 Familial cerebral cavernous malformation
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Transverse limb deficiency-hemangioma syndrome | |
| fr | Syndrome d'anomalies transverses des membres-hémangiome | |
| de | Transversale Extremitätenfehlbildungen-Hämangiom-Syndrom | |
| es | Síndrome de anomalía de las extremidades transversa-hemangioma | |
| it | Anomalie trasversali degli arti - emangioma | |
| nl | Dwarse ledemaatdeficiëntie - hemangioom-syndroom | |
| pt | Síndrome de defeitos transversais dos membros-hemangioma | |
| pl | Skrócenie poprzeczne kończyn - hemangioma | |
| cs | Syndrom zahrnující transverzální končetinový deficit a hemangiom | |
| uk | Синдром поперечної гемангіоми кінцівок | |
| zh | 横向肢端骨缺损-血管瘤综合征 | |
| tr | Transvers ekstremite eksikliği-hemanjiyom sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/2486
- This record as JSON: /data/d/2486.json