raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:268874

OBSOLETE: Congenital hydromyelia

inactive · referred to ORPHA:99856Primary syringomyelia

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 Primary syringomyelia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital hydromyelia
frOBSOLETE : Hydromyélie congénitale
deOBSOLET: Hydromyelie, kongenitale
esOBSOLETO: Hidromielia congénita
itOBSOLETO: Idromielia congenita
nlOBSOLEET: Congenitale hydromyelie
ptOBSOLETO: Hidromielia congénita
plNIEAKTUALNE: Wodordzenie wrodzone
csNEAKTUÁLNÍ: Vrozená hydromyelie
ukЗАСТАРІЛО: Вроджена гідромієлія
zh弃用:先天性脊髓积水
trEski adı: Doğumsal hidromiyeli
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