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Ocular motility disease

MONDO:0001584

65 clinical trials for this condition and its sub-types, 4 tagged with Ocular motility disease itself.

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Where it sits in the disease tree

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Part of

↑ Cranial nerve neuropathy (392)

Sub-types of Ocular motility disease

Strabismus 28 trials · 46 incl. sub-types
11 sub-types
- Exotropia 9 trials · 19 incl. sub-types Sub-types →
- Intermittent squint 14 trials
- Esotropia 8 trials Sub-types →
- Internuclear ophthalmoplegia 3 trials
- Conjugate gaze palsy 1 trial
- Mechanical strabismus 0 trials · 1 incl. sub-types Sub-types →
- Cyclotropia 0 trials
- Hypertropia 0 trials
- Hypotropia 0 trials
- Monofixation syndrome 0 trials
- Paralytic strabismus 0 trials
Ophthalmoplegia 0 trials · 11 incl. sub-types
3 sub-types
- Progressive external ophthalmoplegia 4 trials · 8 incl. sub-types Sub-types →
- Internuclear ophthalmoplegia 3 trials
- Exophthalmic ophthalmoplegia 0 trials
Pathologic nystagmus 7 trials · 9 incl. sub-types
3 sub-types
- Congenital nystagmus 4 trials · 5 incl. sub-types Sub-types →
- Spontaneous ocular nystagmus 2 trials
- Dissociated nystagmus 0 trials
Tolosa-Hunt syndrome 1 trial
Congenital fibrosis of extraocular muscles 1 trial
8 sub-types
- Tukel syndrome 0 trials
- Congenital fibrosis of extraocular muscles type 1 0 trials
- Fibrosis of extraocular muscles, congenital, 2 0 trials
- Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement 0 trials
- Fibrosis of extraocular muscles, congenital, 3b 0 trials
- Fibrosis of extraocular muscles, congenital, 3c 0 trials
- Fibrosis of extraocular muscles, congenital, 5 0 trials
- Fibrosis of extraocular muscles, congenital, with synergistic divergence 0 trials
Weber syndrome 0 trials

Most studied deeper sub-types

Alternating exotropia (11) Kearns-Sayre syndrome (5) Accommodative esotropia (1) Alternating esotropia (1) Autosomal dominant progressive external ophthalmoplegia (1) Brown syndrome (1) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2 (1) Spinocerebellar ataxia 27A (1) Autosomal recessive progressive external ophthalmoplegia (0) Mitochondrial DNA deletion syndrome with progressive myopathy (0) Monocular esotropia (0) Monocular exotropia (0) Nystagmus 1, congenital, X-linked (0) Nystagmus 2, congenital, autosomal dominant (0) Nystagmus 3, congenital, autosomal dominant (0) Nystagmus 5, congenital, X-linked (0) Nystagmus 6, congenital, X-linked (0) Nystagmus 7, congenital, autosomal dominant (0) Nystagmus, congenital, autosomal recessive (0) Nystagmus, hereditary vertical (0)

Including sub-types (65) Tagged with Ocular motility disease (4)

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