raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295181

OBSOLETE: Postaxial polydactyly of toes, bilateral

inactive · referred to ORPHA:498467Non-syndromic postaxial polydactyly

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 Non-syndromic postaxial polydactyly

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Postaxial polydactyly of toes, bilateral
frOBSOLETE : Polydactylie postaxiale bilatérale des orteilsOBSOLETE : Polydactylie postaxiale bilatérale du pied
deOBSOLET: Postaxiale Polydaktylie der Zehen, bilateral
esOBSOLETO: Polidactilia postaxial bilateral de los dedos del pie
itOBSOLETO: Polidattilia postassiale bilaterale delle dita dei piedi
nlOBSOLEET: Postaxiale polydactylie van tenen, bilateraal
ptOBSOLETO: Polidactilia pós-axial dos dedos do pé, bilateral
plNIEAKTUALNE: Polidaktylia pozaosiowa palców stopy, obustronna
csNEAKTUÁLNÍ: Bilaterální postaxiální polydaktylie prstů u nohou
ukЗАСТАРІЛО: Постаксіальна полідактилія пальців стопи, двостороння
zh弃用:双侧趾后多指畸形
trEski adı: Ayak parmakların postaksiyal polidaktilisi, bilateral
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card