raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:498464

Non-syndromic preaxial polydactyly

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNon-syndromic preaxial polydactyly
frPolydactylie préaxiale non syndromique
dePolydaktylie, präaxiale, nicht-syndromale
esPolidactilia preaxial no sindrómica
itPolidattilia preassiale non sindromica
nlNiet-syndromale preaxiale polydactylie
ptPolidactilia pré-axial não sindromática
plNiesyndromiczna polidaktylia przedosiowa
csNesyndromická preaxiální polydaktylie
ukНесиндромальна преаксіальна полідактилія
zh非综合征性轴前多指症
trSendromik olmayan preaksiyal polidaktili
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681229Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (4):

Codes that Orphanet moved or referred to this one:

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