raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295152

OBSOLETE: Polydactyly of an index finger, unilateral

inactive · referred to ORPHA:93337Polydactyly of an index finger

Synonyms: OBSOLETE: Preaxial polydactyly type 3, 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 Polydactyly of an index finger

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Polydactyly of an index finger, unilateralOBSOLETE: Preaxial polydactyly type 3, unilateral
frOBSOLETE : Polydactylie préaxiale type 3, unilatéraleOBSOLETE : Polydactylie de l'index, unilatérale
deOBSOLET: Polydaktylie des Zeigefingers, unilateralOBSOLET: Präaxiale Polydaktylie Typ 3, unilateral
esOBSOLETO: Polidactilia unilateral del dedo índiceOBSOLETO: Polidactilia preaxial unilateral tipo 3
itOBSOLETO: Polidattilia di un indice, unilateraleOBSOLETO: Polidattilia preassiale tipo 3, unilaterale
nlOBSOLEET: Polydactylie van wijsvinger, unilateraalOBSOLEET: Preaxiale polydactylie type 3, unilateraal
ptOBSOLETO: Polidactilia de um dedo indicador, unilateralOBSOLETO: Polidactilia pré-axial tipo 3, bilateral
plNIEAKTUALNE: Polidaktylia palca wskazujacego, jednostronnaNIEAKTUALNE: Polidaktylia przedosiowa typu 3, obustronna
csNEAKTUÁLNÍ: Unilaterální polydaktylie ukazováčkuNEAKTUÁLNÍ: Unilaterální preaxiální polydaktylie, typ 3
ukЗАСТАРІЛО: Полідактилія вказівного пальця, односторонняЗАСТАРІЛО: Преаксіальна полідактилія, тип 3, одностороння
zh弃用:单侧食指多指畸形单侧轴前多指畸形3型
trEski adı: İşaret parmak polidaktilisi, unilateralPreaksiyel polidaktili tip 3, 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