raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:268770

OBSOLETE: Upper thoracic 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: Upper thoracic spina bifida cystica
frOBSOLETE : Spina bifida kystique thoracique supérieurOBSOLETE : Spina bifida cystica thoracique supérieure
deOBSOLET: Spina bifida cystica, obere thorakale
esOBSOLETO: Espina bífida quística torácica superior
itOBSOLETO: Spina bifida cistica toracica superiore
nlOBSOLEET: Boventhoracale spina bifida cystica
ptOBSOLETO: Espinha bífida quística torácica superior
plNIEAKTUALNE: Torbielowaty rozszczep górnego odcinka kręgosłupa piersiowego
csNEAKTUÁLNÍ: Horní hrudní spina bifida cystica
ukЗАСТАРІЛО: Кістозне розщеплення верхньогрудного відділу хребта (spina bifida cystica)
zh上胸部囊性脊柱裂
trÜst torasik 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