Please sign in to follow a disease.

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary neurological disease (5791) ↑ Congenital nervous system disorder (287) ↑ 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! 2 Completed 2

Congenital nystagmus

Where it sits in the disease tree

AR glasses may revolutionize vertigo diagnosis

Scientists hunt for Eye-Misalignment genes