raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:435808

OBSOLETE: ACAN-related skeletal dysplasia

inactive · referred to ORPHA:674499Proteoglycan-related bone disorder

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 Proteoglycan-related bone disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: ACAN-related skeletal dysplasia
frOBSOLETE : Dysplasie squelettique associée à ACAN
deOBSOLET: ACAN-assoziierte Skelettdysplasie
esOBSOLETO: Displasia esquelética asociada a ACAN
itOBSOLETO: Displasia scheletrica ACAN-correlata
nlOBSOLEET: ACAN-gerelateerde skeletdysplasie
ptOBSOLETO: Displasia esquelética ACAN-relacionada
plNIEAKTUALNE: Dysplazja szkieletowa zwiazana z ACAN
csNEAKTUÁLNÍ: ACAN-vázaná skeletální dysplázie
ukЗАСТАРІЛО: ACAN-асоційована скелетна дисплазія
zh弃用:ACAN相关性骨骼发育不良
trEski adı: ACAN-ilişkili iskelet displazisi
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