raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:268748

OBSOLETE: Total spina bifida cystica

inactive · referred to ORPHA:268744Spinal dysraphism with a posterior meningocele

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Spinal dysraphism with a posterior meningocele

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Total spina bifida cystica
frOBSOLETE : Spina bifida kystique completOBSOLETE : Spina bifida cystica complète
deOBSOLET: Spina bifida cystica, totale
esOBSOLETO: Espina bífida quística total
itOBSOLETO: Spina bifida cistica completa
nlOBSOLEET: Volledige spina bifida cystica
ptOBSOLETO: Espinha bífida quística total
plNIEAKTUALNE: Całkowity torbielowaty rozszczep kręgosłupa
csNEAKTUÁLNÍ: Totální spina bifida cystica
ukЗАСТАРІЛО: Тотальне кістозне розщеплення хребта (spina bifida cystica)
zh全囊性脊柱裂
trTotal spina bifida sistika
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