raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:519337

Disorder with optic nerve compression

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enDisorder with optic nerve compression
frMaladie avec compression du nerf optique
deErkrankung mit Kompression des Nervus opticus
esTrastorno con compresión del nervio óptico
itPatologia con compressione del nervo ottico
nlAandoening met compressie van oogzenuw
ptDoença com compressão do nervo óptico
plChoroba przebiegająca z uciskiem nerwu wzrokowego
csPorucha s kompresí zrakového nervu
ukПорушення з компресією зорового нерва
zh视神经压迫症
trOptik sinir sıkışması ile seyreden bozukluk
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (2):

Children (2):

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