raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:329252

OBSOLETE: Spondylocostal dysostosis-hypospadias-intellectual disability syndrome

inactive · referred to ORPHA:93454Dysostosis with predominant vertebral and costal involvement

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 Dysostosis with predominant vertebral and costal involvement

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Spondylocostal dysostosis-hypospadias-intellectual disability syndrome
frOBSOLETE : Syndrome de dysostose spondylocostale-hypospadias-déficience intellectuelle
deOBSOLET: Spondylokostale Dysostose-Hypospadie-Intelligenzminderung-Syndrom
esOBSOLETO: Síndrome de disostosis espondilocostal-hipospadias-discapacidad intelectual
itOBSOLETO: Sindrome da disostosi spondilocostale, ipospadia e disabilità intelletiva
nlOBSOLEET: Spondylocostale dysostose - hypospadie - intellectuele achterstand-syndroom
ptOBSOLETO: Síndrome de disostose espondilocostal-hipospádias-perturbação do desenvolvimento intelectual
plNIEAKTUALNE: Dyzostoza kręgowo-żebrowa - spodziectwo - niepełnosprawność intelektualna
csNEAKTUÁLNÍ: Syndrom zahrnující spondylokostální dysostózu, hypospadii a mentální retardaci
ukЗАСТАРІЛО: Синдром спондилокостального дизостозу-гіпоспадії-інтелектуальної недостатності
zh脊椎肋骨发育不良-尿道下裂-智力障碍综合征
trSpondilokostal dizostoz-hipospadias-zihinsel yetersizlik sendromu

Definition in:

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.

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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.

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Sources for this card