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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
agenesis of corpus callosum, cardiac, ocular, and genital syndrome  
amblyopia +   
ancylostomiasis +  
Asthenopia  
autoimmune disease of central nervous system +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
baylisascariasis 
blindness +   
brain disease +   
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
Cogan syndrome +   
conjunctival disease +   
corneal disease +   
CRANIAL DYSINNERVATION DISORDER, CONGENITAL, WITH ABSENT CORNEAL REFLEX AND DEVELOPMENTAL DELAY  
Cranial Nerve Injuries +   
Cranial Nerve Neoplasms +   
cranial nerve palsy +  
Cranial Nerves, Congenital Paresis of 
Cranial Nerves, Recurrent Paresis of 
cysticercosis +  
dipetalonemiasis 
Encephalocraniocutaneous Lipomatosis  
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
Eye Abnormalities +   
eye accommodation disease +  
eye adnexa disease +   
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
facial nerve disease +   
Flynn Aird Syndrome 
fundus dystrophy +   
glaucoma +   
globe disease +   
glossopharyngeal nerve disease +   
gonorrhea +  
hemiplegia +   
Hereditary Eye Diseases +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
high pressure neurological syndrome 
hyperekplexia +   
hypoglossal nerve disease +   
intracranial abscess 
jaw-winking syndrome  
lacrimal apparatus disease +   
lens disease +   
leprosy +   
loiasis 
Marfan syndrome +   
maturity-onset diabetes of the young type 5  
meningitis +   
microphthalmia +   
Mollica-Pavone-Antener Syndrome 
MORM Syndrome  
movement disease +   
neurodegenerative disease +   
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Neuromuscular Oculoauditory Syndrome  
neuronitis 
neurosarcoidosis +  
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Disorders that feature impairment of eye movements as a primary manifestation of disease. These conditions may be divided into infranuclear, nuclear, and supranuclear disorders. Diseases of the eye muscles or oculomotor cranial nerves (III, IV, and VI) are considered infranuclear. Nuclear disorders are caused by disease of the oculomotor, trochlear, or abducens nuclei in the BRAIN STEM. Supranuclear disorders are produced by dysfunction of higher order sensory and motor systems that control eye movements, including neural networks in the CEREBRAL CORTEX; BASAL GANGLIA; CEREBELLUM; and BRAIN STEM. Ocular torticollis refers to a head tilt that is caused by an ocular misalignment. Opsoclonus refers to rapid, conjugate oscillations of the eyes in multiple directions, which may occur as a parainfectious or paraneoplastic condition (e.g., OPSOCLONUS-MYOCLONUS SYNDROME). (Adams et al., Principles of Neurology, 6th ed, p240)
Ocular Neovascularization +   
ocular sarcoidosis  
OCULOMOTOR-ABDUCENS SYNKINESIS  
olfactory nerve disease +   
ophthalmia nodosa 
ophthalmomyiasis 
Ophthalmoplegic Migraine 
optic nerve disease +   
orbital disease +   
paraplegia +   
philophthalmiasis 
Pneumocephalus 
pupil disease +   
quadriplegia +   
refractive error +   
retinal disease +   
scleral disease +   
scotoma +   
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal  
spinal cord disease +   
third cranial nerve disease +   
toxocariasis +   
trigeminal nerve disease +   
trochlear nerve disease +  
uveal disease +   
Vagus nerve disease +   
vestibulocochlear nerve disease +   
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   

Synonyms
Exact Synonyms: Convergence Excess ;   Convergence Excesses ;   Convergence Insufficiencies ;   Convergence Insufficiency ;   Cyclophoria ;   Cyclophorias ;   Eye Motility Disorder ;   Eye Motility Disorders ;   Eye Movement Disorder ;   Eye Movement Disorders
Primary IDs: MESH:D015835
Xrefs: EFO:1001990 ;   GARD:7061 ;   GARD:7237 ;   ICD9CM:378.9

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