raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:235838

OBSOLETE: Congenital vascular bone syndrome with limb shortening

inactive · referred to ORPHA:235832Congenital vascular bone syndrome

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 Congenital vascular bone syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital vascular bone syndrome with limb shortening
frOBSOLETE : Syndrome vasculaire osseux congénital avec raccourcissement d'un membre
deOBSOLET: Gefäßknochensyndrom, kongenitales, mit vermindertem Wachstum der Extremitäten
esOBSOLETO: Síndrome óseo vascular congénito con acortamiento de las extremidades
itOBSOLETO: Sindrome vascolare ossea congenita con accorciamento degli arti
nlOBSOLEET: Congenitaal vasculair botsyndroom met lengtedefect van ledematen
ptOBSOLETO: Síndrome congénito de osso vascular com encurtamento dos membros
plNIEAKTUALNE: Wrodzony zespól waskularyzacji kosci ze skróceniem konczyn
csNEAKTUÁLNÍ: Congenital vascular bone syndrome with limb shortening
ukЗАСТАРІЛО: Вроджений судинно-кістковий синдром з вкороченням кінцівок
zh弃用:先天性血管骨综合征伴肢体缩短
trEski adı: Ekstremite kısalması ile seyreden doğumsal vasküler kemik sendromu
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