raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:294961

OBSOLETE: Syndromes with synostoses of limbs

inactive · referred to ORPHA:93459Syndrome with synostosis or other joint formation defect

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 Syndrome with synostosis or other joint formation defect

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Syndromes with synostoses of limbs
frOBSOLETE : Syndromes avec synostose des membresOBSOLETE : Syndromes avec fusion des membres
deOBSOLET: Syndrome mit Synostosee der Extremitäten
esOBSOLETO: Síndromes con sinostosis de extremidades
itOBSOLETO: Sindromi con sinostosi degli arti
nlOBSOLEET: Syndromen met synostosen van ledematen
ptOBSOLETO: Síndromes com sinostoses dos membros
plNIEAKTUALNE: Zespoly z synostoza konczyn
csNEAKTUÁLNÍ: Syndromy se synostózami končetin
ukЗАСТАРІЛО: Синдроми з синостозами кінцівок
zh弃用:四肢骨性连结综合征
trEski adı: Ekstremitelerin sinostoz ile seyreden sendromları
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