raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:295167

OBSOLETE: Postaxial polydactyly type B, unilateral

inactive · referred to ORPHA:93335Postaxial polydactyly type B

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 Postaxial polydactyly type B

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Postaxial polydactyly type B, unilateral
frOBSOLETE : Polydactylie postaxiale type B, unilatérale
deOBSOLET: Postaxiale Polydaktylie Typ B, unilateral
esOBSOLETO: Polidactilia postaxial unilateral tipo B
itOBSOLETO: Polidattilia postassiale unilaterale, tipo B
nlOBSOLEET: Postaxiale polydactylie type B, unilateraal
ptOBSOLETO: Polidactilia pós-axial tipo B, unilateral
plNIEAKTUALNE: Polidaktylia pozaosiowa typu B, jednostronna
csNEAKTUÁLNÍ: Unilaterální postaxiální polydaktylie, typ B
ukЗАСТАРІЛО: Постаксіальна полідактилія, тип В, одностороння
zh弃用:单侧B型后肢多指畸形
trEski adı: Postaksiyal polidaktili tip B, 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