ORPHA:295136
OBSOLETE: Symbrachydactyly of hand and foot, unilateral
inactive · referred to ORPHA:498451Dysostosis with brachydactyly without extraskeletal manifestations
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Dysostosis with brachydactyly without extraskeletal manifestations
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Symbrachydactyly of hand and foot, unilateral | |
| fr | OBSOLETE : Symbrachydactylie de la main et du pied, unilatérale | |
| de | OBSOLET: Symbrachydakytlie der Hände und Füße, unilateral | |
| es | OBSOLETO: Simbraquidactilia unilateral de manos y pies | |
| it | OBSOLETO: Sinbrachidattilia unilaterale della mano e del piede | |
| nl | OBSOLEET: Symbrachydactylie van hand en voet, unilateraal | |
| pt | OBSOLETO: Simbraquidactilia da mão e do pé, unilateral | |
| pl | NIEAKTUALNE: Symbrachydaktylia dloni i stóp, jednostronna | |
| cs | NEAKTUÁLNÍ: Unilaterální symbrachydaktylie prstů ruky a nohy | |
| uk | ЗАСТАРІЛО: Симбрахідактилія кисті та стопи, одностороння | |
| zh | 弃用：单侧手足指/趾交叉 | |
| tr | Eski adı: El ve ayak simbrakidaktilisi, unilateral |
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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/295136
- This record as JSON: /data/d/295136.json