ORPHA:3332
Hypoplastic tibiae-postaxial polydactyly syndrome
inactive · moved to ORPHA:988Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
Synonyms: Hypoplastic tibia-polydactyly syndrome · Werner mesomelic 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 Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hypoplastic tibiae-postaxial polydactyly syndrome | Hypoplastic tibia-polydactyly syndrome · Werner mesomelic syndrome |
| fr | Syndrome de tibia hypoplasique-polydactylie | Syndrome mésomélique de Werner |
| de | Hypoplastische Tibia-postaxiale Polydaktylie-Syndrom | Werner mesomeles Syndrom |
| es | Síndrome de hipoplasia tibial-polidactilia postaxial | Síndrome de hipoplasia tibial-polidactilia · Síndrome mesomélico de Werner |
| it | Sindrome da ipoplasia della tibia-polidattilia postassiale | Sindrome da ipoplasia della tibia-polidattilia · Sindrome mesomelica di Werner |
| nl | Hypoplastische tibiae - postaxiale polydactylie-syndroom | Hypoplastisch scheenbeen - polydactylie-syndroom · Mesomeel syndroom van Werner |
| pt | Síndrome de tíbias hipoplásicas-polidactilia pós-axial | Síndrome de tíbia hipoplásica-polidactilia · Síndrome mesomélico Werner |
| pl | Niedorozwój kości promieniowej - polidaktylia pozaosiowa | Mezomeliczny zespół Wernera · Zespół hipoplastycznej kości piszczelowej i polidaktylii pozaosiowej |
| cs | Syndrom zahrnující hypoplastické tibie a postaxiální polydaktylii | Wernerův mezomelický syndrom |
| uk | Синдром гіпопластичної великогомілкової кістки-постаксіальної полідактилії | Синдром гіпопластичної полідактилії великогомілкової кістки · Мезомелічний синдром Вернера |
| zh | 胫骨发育不全-轴后性多指症综合征 | 胫骨发育不全-多指综合征 |
| tr | Hipoplastik tibiae-postaksiyal polidaktili sendromu | Werner mezomelik sendromu · Hipoplastik tibia-polidaktili sendromu |
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/3332
- This record as JSON: /data/d/3332.json