Ocular motility disease
MONDO:000158465 clinical trials for this condition and its sub-types, 4 tagged with Ocular motility disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
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
-
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)