Congenital abducens nerve palsy

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Congenital abducens nerve palsy

ORPHA:440233Disease

Also called Benign congenital sixth cranial nerve palsy · Congenital CNVI palsy

What it is

A rare neuro-ophthalmological disease characterized by dysfunction of the ipsilateral lateral rectus muscle with esotropia in primary position, limited or no abduction of the eyeball, and compensatory horizontal face turn toward the palsied eye. The condition commonly resolves spontaneously.

Key facts

Age of onset
Neonatal
Inheritance
Not applicable
Classified as
Disease

ICD-10 codes

Q07.8filed under a broader ICD-10 category — shared with 14 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MONDO 0018600UMLS C1302994

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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