raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:139018

OBSOLETE: Non-chondrodysplastic malformation syndrome affecting bones

inactive · referred to ORPHA:139012Rare bone development 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 Rare bone development disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Non-chondrodysplastic malformation syndrome affecting bones
frOBSOLETE : Syndrome malformatif non-chondrodysplasique avec anomalies osseuses
deOBSOLET: Dysmorphie-Syndrom mit Knochenbeteiligung, nicht-chondrodysplastisch
esOBSOLETO: Síndrome malformativo que afecta huesos, no condrodisplásico
itOBSOLETO: Sindrome dismorfica non condrodisplasica con anomalie scheletriche
nlOBSOLEET: Niet-chondrodysplastisch malformatiesyndroom met aantasting van bot
ptOBSOLETO: Síndrome dismórfico com envolvimento ósseo, não-condrodisplástico
plNIEAKTUALNE: Zespól malformacji niechondrodysplastycznej dotyczacy kosci
csNEAKTUÁLNÍ: Syndrom nechondrodysplastické malformace postihující kosti
ukЗАСТАРІЛО: Синдром нехондродиспластичної мальформації, що вражає кістки
zh弃用:影响骨骼的非软骨发育不良型畸形综合征
trEski adı: Kemikleri etkileyen kondrodisplastik olmayan malformasyon 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