raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93456

OBSOLETE: Brachydactyly group

inactive · referred to ORPHA:69028Dysostosis with brachydactyly

Synonyms: OBSOLETE: Brachydactyly with or without extraskeletal manifestations

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Dysostosis with brachydactyly

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Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Brachydactyly groupOBSOLETE: Brachydactyly with or without extraskeletal manifestations
frOBSOLETE : BrachydactyliesOBSOLETE : Brachydactylie avec ou sans manifestations extra squelettiques
deOBSOLET: BrachydaktylieOBSOLET: Brachydaktylie mit oder ohne extraskelettale Manifestationen
esOBSOLETO: Braquidactilia (grupo de enfermedades)OBSOLETO: Braquidactilia con o sin manifestaciones extraesqueléticas
itOBSOLETO: BrachidattilieOBSOLETO: Brachidattilia con o senza segni clinici extrascheletrici
nlOBSOLEET: BrachydactyliegroepOBSOLEET: Brachydactylie met of zonder extraskeletale manifestaties
ptOBSOLETO: Braquidactilias
plNIEAKTUALNE: Grupa brachydaktyliiNIEAKTUALNE: Brachydaktylia z objawami pozaszkieletowymi lub bez objawów pozaszkieletowych
csNEAKTUÁLNÍ: Brachydaktylická skupina= en
ukЗАСТАРІЛО: Група брахідактиліїЗАСТАРІЛО: Брахідактилія з екстраскелетними проявами або без них
zh弃用:短指(趾)畸形类疾病短指(趾)畸形伴/不伴骨外表现
trEski adı: Brakidaktili grubuEkstraskeletal belirtiler ile seyreden veya seyretmeyen brakidaktili
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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.

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Sources for this card