raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295179

OBSOLETE: Postaxial polydactyly of toes, unilateral

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, unilateral
frOBSOLETE : Polydactylie postaxiale unilatérale des orteilsOBSOLETE : Polydactylie postaxiale unilatérale du pied
deOBSOLET: Postaxiale Polydaktylie der Zehen, unilateral
esOBSOLETO: Polidactilia postaxial unilateral de los dedos del pie
itOBSOLETO: Polidattilia postassiale unilaterale delle dita dei piedi
nlOBSOLEET: Postaxiale polydactylie van tenen, unilateraal
ptOBSOLETO: Polidactilia pós-axial dos dedos do pé, unilateral
plNIEAKTUALNE: Polidaktylia pozaosiowa palców stopy, jednostronna
csNEAKTUÁLNÍ: Unilaterální postaxiální polydaktylie prstů u nohou
ukЗАСТАРІЛО: Постаксіальна полідактилія пальців стопи, одностороння
zh弃用:单侧趾后多指畸形
trEski adı: Ayak parmakların postaksiyal polidaktilisi, unilateral
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