raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:100932

OBSOLETE: Nuclear oculomotor paralysis

inactive · referred to ORPHA:519349Rare ophthalmic disorder with cranial nerve involvement

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare ophthalmic disorder with cranial nerve involvement

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Nuclear oculomotor paralysis
frOBSOLETE : Paralysie oculomotrice nucléaire
deOBSOLET: Supranukleäre Blickparese
esOBSOLETO: Parálisis oculomotora nuclear
itOBSOLETO: Paralisi oculomotoria nucleare
nlOBSOLEET: Nucleaire oculomotorische paralyseOBSOLEET: Nucleaire oculomotorische verlamming
ptOBSOLETO: Paralisia oculomotora nuclear
plNIEAKTUALNE: Porazenie jadra nerwu okoruchowego
csNEAKTUÁLNÍ: Nukleární okulomotorická paralýza
ukЗАСТАРІЛО: Ядерний окоруховий параліч
zh弃用:核动眼神经麻痹
trEski adı: Nükleer okülomotor paraliz
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