raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93435

OBSOLETE: Moderate spondylodysplastic dysplasia

inactive · referred to ORPHA:93434Spondylodysplastic dysplasia

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 Spondylodysplastic dysplasia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Moderate spondylodysplastic dysplasia
frOBSOLETE : Dysplasie spondylo-dysplasique modérée
deOBSOLET: Dysplasie, spondylodysplastische, moderate
esOBSOLETO: Displasia espondiloplástica moderada
itOBSOLETO: Displasia spondilodisplastica moderata
nlOBSOLEET: Matige spondylodysplastische dysplasie
ptOBSOLETO: Displasia espondilodisplásica moderada
plNIEAKTUALNE: Umiarkowana dysplazja kregoslupowo-dysplastyczna
csNEAKTUÁLNÍ: Středně těžká spondylodysplastická dysplázie
ukЗАСТАРІЛО: Помірна спондилодиспластична дисплазія
zh弃用:轻度脊柱发育不良
trEski adı: Orta derecede spondilodisplastik 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