raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:163678

OBSOLETE: Unclassified spondylometaphyseal dysplasia

inactive · referred to ORPHA:254Spondylometaphyseal dysplasia

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Unclassified spondylometaphyseal dysplasia
frOBSOLETE : Dysplasie spondylo-métaphysaire non classifiée
deOBSOLET: Dysplasie, spondylometaphysäre (weitere Typen)
esOBSOLETO: Displasia espondiloepifisaria no clasificada
itOBSOLETO: Displasia spondiloepifisaria non classificata
nlOBSOLEET: Niet-geclassificeerde spondylo-metafysaire dysplasie
ptOBSOLETO: Displasia espondilometafisária, outros tipos
plNIEAKTUALNE: Niesklasyfikowana dysplazja przynasadowa
csNEAKTUÁLNÍ: Neklasifikovaná spondylometafyzální dysplázie
ukЗАСТАРІЛО: Некласифікована спондилометафізарна дисплазія
zh弃用:未分类的脊椎间隙发育不良
trEski adı: Sınıflandırılmamış spondilometafizyal displazi
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