raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93968

Meningocele

inactive · moved to ORPHA:823Spina bifida and other spinal dysraphisms

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Isolated spina bifida

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMeningocele
frMéningocèle
deMeningozele
esMeningocele
itMeningocele
nlMeningocele
ptMeningocelo
plPrzepuklina oponowa
csMeningokéla
ukМенінгоцеле
zh脑脊膜膨出
trMeningosel
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MeSHD008588Evalidated
GARD3471Evalidated
MedDRA10027266Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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