raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:268871

OBSOLETE: Primary syringomyelia/hydromyelia

inactive · referred to ORPHA:99856Primary syringomyelia

Type
Morphological anomaly
Group
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: Primary syringomyelia/hydromyelia
frOBSOLETE : Syringomyélie/hydromyélie primitive
deOBSOLET: Syringomyelie/Hydromelie, primäre
esOBSOLETO: Siringomielia/hidromielia primaria
itOBSOLETO: Siringomielia/idromielia primitiva
nlOBSOLEET: Primaire syringomyelie/hydromyelie
ptOBSOLETO: Siringomielia/hidromielia primária
plNIEAKTUALNE: Pierwotna jamistosc rdzenia/wodordzenie
csNEAKTUÁLNÍ: Primární syringomyelie/hydromyelie
ukЗАСТАРІЛО: Первинна сирингомієлія/гідромієлія
zh弃用:原发性脊髓空洞症/脊髓积水
trEski adı: Primer siringomiyeli/hidromeli
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