raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295144

OBSOLETE: Polydactyly of a biphalangeal thumb, unilateral

inactive · referred to ORPHA:93339Polydactyly of a biphalangeal thumb and/or hallux

Synonyms: OBSOLETE: Preaxial polydactyly type 1, 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 a biphalangeal thumb and/or hallux

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Polydactyly of a biphalangeal thumb, unilateralOBSOLETE: Preaxial polydactyly type 1, unilateral
frOBSOLETE : Polydactylie d'un pouce biphalangé, unilatéraleOBSOLETE : Polydactylie préaxiale type 1, unilatérale
deOBSOLET: Polydaktylie eines biphalangealen Daumens, unilateralOBSOLET: Präaxiale Polydaktylie Typ 1, unilateral
esOBSOLETO: Polidactilia unilateral del pulgar bifalángicoOBSOLETO: Polidactilia preaxial unilateral tipo 1
itOBSOLETO: Polidattilia del pollice bifalangeo, unilateraleOBSOLETO: Polidattilia preassiale tipo 1, unilaterale
nlOBSOLEET: Polydactylie van bifalangeale duim, unilateraalOBSOLEET: Preaxiale polydactylie type 1, unilateraal
ptOBSOLETO: Polidactilia do polegar, unilateralOBSOLETO: Polidactilia pré-axial tipo 1, unilateral
plNIEAKTUALNE: Polidaktylia dwupaliczkowego kciuka, jednostronnaNIEAKTUALNE: Polidaktylia przedosiowa typu 1, jednostronna
csNEAKTUÁLNÍ: Unilaterální polydaktylie bifalangeálního palceNEAKTUÁLNÍ: Unilaterální preaxiální polydaktylie, typ 1
ukЗАСТАРІЛО: Полідактилія двофалангового великого пальця, односторонняЗАСТАРІЛО: Преаксіальна полідактилія, тип 1, одностороння
zh弃用:单侧双指拇指多指畸形单侧轴前多指畸形1型
trEski adı: Bifalanjiyal başparmak polidaktilisi, unilateralPreaksiyel polidaktili tip 1, 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