raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93458

Non-syndromic polydactyly, syndactyly and/or hyperphalangy

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 polydactyly, syndactyly and/or hyperphalangy
frPolydactylie, syndactylie et/ou hyperphalangie non syndromique
dePolydaktylie, Syndaktylie und/oder Hyperphalangie, nicht-syndromal
esPolidactilia, sindactilia y/o hiperfalangismo no sindrómico
itPolidattilia, sindattilia e/o iperfalangia non sindromica
nlNiet-syndromale polydactylie, syndactylie en/of hyperfalangie
ptPolidactialia, sindactilia e/ou hiperfalangismo não sindromáticos
plPolidaktylia, syndaktylia i/lub hiperfalangia
csNesyndromické polydaktylie, syndaktylie a/nebo hyperfalangie
ukНесиндромна полідактилія, синдактилія та/або гіперфалангія
zh非综合征型多指（趾）和/或并指（趾）
trNon-Sendromik polidaktili, sindaktili ve / veya hiperfalji
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681597Evalidated

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 (3):

Children (3):

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