raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93472

OBSOLETE: Dysmorphic syndrome associated with bone anomaly

inactive · referred to ORPHA:68341Multiple congenital anomalies/dysmorphic 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 Multiple congenital anomalies/dysmorphic syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Dysmorphic syndrome associated with bone anomaly
frOBSOLETE : Syndrome dysmorphique avec atteinte osseuse
deOBSOLET: Dysmorphie-Syndrom mit assoziierter Knochenanomalie
esOBSOLETO: Síndrome dismorfológico asociado a anomalías óseas
itOBSOLETO: Sindrome dismorfica associata a anomalie ossee
nlOBSOLEET: Dysmorfie-syndroom geassocieerd met botanomalie
ptOBSOLETO: Síndrome dismórfico associado a anomalia óssea
plNIEAKTUALNE: Zespól dysmorficzny z towarzyszaca anomalia kosci
csNEAKTUÁLNÍ: Dysmorfický syndrom spojený s anomálií kostí
ukЗАСТАРІЛО: Дисморфічний синдром, повязаний з кістковою аномалією
zh弃用:骨异常相关畸形综合征
trEski adı: Kemik anomalisi -ilişkili dismorfik sendrom
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