ORPHA:295132
OBSOLETE: Brachydactyly of toes, unilateral
inactive · referred to ORPHA:498451Dysostosis with brachydactyly without extraskeletal manifestations
Synonyms: OBSOLETE: Short toes, unilateral
- 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
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Brachydactyly of toes, unilateral | OBSOLETE: Short toes, unilateral |
| fr | OBSOLETE : Brachydactylie des orteils, unilatérale | OBSOLETE : Orteils courts, unilatéral |
| de | OBSOLET: Brachydakytlie der Zehen, unilateral | OBSOLET: Kurze Zehen, unilateral |
| es | OBSOLETO: Braquidactilia unilateral de los dedos del pie | OBSOLETO: Dedos del pie cortos, unilateral |
| it | OBSOLETO: Brachidattilia delle dita del piede, unilaterale | OBSOLETO: Dita dei piedi corte, forma unilaterale · OBSOLETO: Dita dei piedi corte, unilaterale |
| nl | OBSOLEET: Brachydactylie van tenen, unilateraal | OBSOLEET: Korte tenen, unilateraal |
| pt | OBSOLETO: Braquidactilia dos dedos do pé, unilateral | OBSOLETO: Dedos do pé curtos, unilateral |
| pl | NIEAKTUALNE: Brachydaktylia palców stopy, jednostronna | NIEAKTUALNE: Krótkie palce stopy, jednostronne |
| cs | NEAKTUÁLNÍ: Unilaterální brachydaktylie prstů u nohy | NEAKTUÁLNÍ: Unilaterální krátké prsty u nohou |
| uk | ЗАСТАРІЛО: Брахідактилія пальців ніг, одностороння | ЗАСТАРІЛО: Короткі пальці, односторонні |
| zh | 弃用：单侧脚趾短趾 | 单侧短趾 |
| tr | Eski adı: Ayak parmak brakidaktilisi, unilateral | Kısa ayak parmakları unilateral |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295132
- This record as JSON: /data/d/295132.json