Congenital nystagmus

MONDO:0005712

Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with albinism and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)

Also known as: nystagmus, congenital idiopathic nystagmus, congenital pathologic nystagmus, motor congenital nystagmus, nystagmus, congenital

6 clinical trials for this condition and its sub-types, 4 tagged with Congenital nystagmus itself.

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Where it sits in the disease tree

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↑ Hereditary neurological disease (5772) ↑ Congenital nervous system disorder (284) ↑ Pathologic nystagmus (9)

Sub-types of Congenital nystagmus

Spinocerebellar ataxia 27A 1 trial
Nystagmus 1, congenital, X-linked 0 trials
Nystagmus 2, congenital, autosomal dominant 0 trials
Nystagmus 3, congenital, autosomal dominant 0 trials
Nystagmus 5, congenital, X-linked 0 trials
Nystagmus 6, congenital, X-linked 0 trials
Nystagmus 7, congenital, autosomal dominant 0 trials
Nystagmus, congenital, autosomal recessive 0 trials
Nystagmus, hereditary vertical 0 trials
Nystagmus, myoclonic 0 trials

Including sub-types (6) Tagged with Congenital nystagmus (4)

Trials to join now! 3 Not yet recruiting 1 Completed 2

Your phone camera could soon spot eye disorders

Diagnosis Not yet recruiting

This study will check if an AI system can accurately measure eye movements from smartphone videos. About 1,000 adults with suspected eye movement issues will record a short video while following a moving target. The AI's measurements will be compared to expert ratings to see if i…

Sponsor: THYROSCOPE INC. • Aim: Diagnosis

Last updated Jun 27, 2026 13:01 UTC

Congenital nystagmus

Where it sits in the disease tree

Your phone camera could soon spot eye disorders