ocular motility disorders

Preferred Label : ocular motility disorders;

MeSH definition : 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);

MeSH synonym : ocular motility disorder; eye movement disorders; eye movement disorder; eye motility disorders; eye motility disorder;

MeSH hyponym : spasm of conjugate gaze; pseudoophthalmoplegia; opsoclonus; paroxysmal ocular dyskinesia; cyclophoria; internuclear ophthalmoplegia; ocular torticollis; parinaud syndrome; convergence excess; smooth pursuit deficiency; convergence insufficiency; skew deviation; Convergence Excesses; Excess, Convergence; Convergence Insufficiencies; Insufficiencies, Convergence; Insufficiency, Convergence; Cyclophorias; Internuclear Ophthalmoplegias; Ophthalmoplegia, Internuclear; Ophthalmoplegias, Internuclear; Conjugate Gaze Spasm; Conjugate Gaze Spasms; Gaze Spasms, Conjugate; Syndrome, Parinaud; Parinaud's Syndrome; Parinauds Syndrome; Syndrome, Parinaud's; Dyskinesia, Paroxysmal Ocular; Dyskinesias, Paroxysmal Ocular; Ocular Dyskinesia, Paroxysmal; Ocular Dyskinesias, Paroxysmal; Paroxysmal Ocular Dyskinesias; Pseudoophthalmoplegias; Deviation, Skew; Deviations, Skew; Skew Deviations; Deficiencies, Smooth Pursuit; Pursuit Deficiencies, Smooth; Pursuit Deficiency, Smooth; Smooth Pursuit Deficiencies; Deficiency, Smooth Pursuit;

Related MeSH term : brown tendon sheath syndrome; Syndrome, Brown's Tendon Sheath; Tendon Sheath Syndrome of Brown; Brown's Tendon Sheath Syndrome; Brown's Syndrome; Browns Syndrome; Syndrome, Brown's; Brown Syndrome; Syndrome, Brown;

MeSH annotation : GEN: prefer specifics;

Wikipedia link : https://en.wikipedia.org/wiki/Ocular motility disorder;

Details

Origin ID

D015835;

UMLS CUI

C0028850;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Brown syndrome [PASCAL descriptor]
- Brown syndrome [OMIM Phenotype]
- Brown's (tendon) sheath syndrome [ICD-9 code]
- Brown's (tendon) sheath syndrome [MedDRA LLT]
- Brown's sheath syndrome [ICD-11 More detail]
- Convergence excess [ICD-11 Subcategory]
- Convergence excess (disorder) [SNOMED CT concept]
- Convergence insufficiency [PASCAL descriptor]
- Convergence insufficiency [ICD-11 Subcategory]
- Convergence insufficiency [MedDRA LLT]
- Convergence insufficiency (disorder) [SNOMED CT concept]
- Convergence spasm (disorder) [SNOMED CT concept]
- Cyclophoria [PASCAL descriptor]
- Cyclophoria [ICD-11 More detail]
- Cyclophoria [HPO term]
- Cyclophoria [ICD-9 code]
- Cyclophoria [MedDRA LLT]
- Cyclophoria (disorder) [SNOMED CT concept]
- Dorsal midbrain syndrome [ICD-11 More detail]
- Eye movement disorder NOS [MedDRA LLT]
- Eye movement disorders [MedDRA High Level Term]
- Hertwig-Magendie syndrome [PASCAL descriptor]
- Heterophoria [ICD-10 Sub-category (who)]
- Impaired convergence [HPO term]
- Internuclear ophthalmoplegia [PASCAL descriptor]
- Internuclear ophthalmoplegia [ICD-10 Sub-category]
- Internuclear ophthalmoplegia [ICD-11 Subcategory]
- Internuclear ophthalmoplegia [HPO term]
- Internuclear ophthalmoplegia [ICD-9 code]
- Internuclear ophthalmoplegia [ICD-10 Sub-category (who)]
- Internuclear ophthalmoplegia [MedDRA LLT]
- Internuclear ophthalmoplegia (disorder) [SNOMED CT concept]
- Mechanical strabismus [ICD-10 Sub-category]
- Mechanical strabismus [ICD-10 Sub-category (who)]
- OPHTHALMOPLEGIA [WHO-ART Included Term]
- Ocular torticollis [PASCAL descriptor]
- Ocular torticollis [ICD-9 code]
- Ocular torticollis [MedDRA Preferred Term]
- Ocular torticollis (disorder) [SNOMED CT concept]
- Ophthalmoplegia [HPO term]
- Ophthalmoplegia [MedDRA Preferred Term]
- Ophthalmoplegia [NCIt concept]
- Ophthalmoplegia (disorder) [SNOMED CT concept]
- Ophthalmoplegia NOS [MedDRA LLT]
- Opsoclonia (finding) [SNOMED CT concept]
- Opsoclonus [PASCAL descriptor]
- Opsoclonus [NCIt concept]
- Opsoclonus [ICD-11 More detail]
- Opsoclonus [HPO term]
- Parinaud Syndrome [NCIt concept]
- Parinaud syndrome [MedDRA Preferred Term]
- Parinaud's syndrome (disorder) [SNOMED CT concept]
- Paroxysmal ocular dyskinesia (disorder) [SNOMED CT concept]
- Pseudoophthalmoplegia (disorder) [SNOMED CT concept]
- Skew deviation [ICD-11 Sub-sub category]
- Skew deviation (disorder) [SNOMED CT concept]
- Spasm of conjugate gaze [ICD-11 Subcategory]
- Spasm of conjugate gaze [ICD-9 code]
- brown's tendon sheath syndrome [SNOMED Notion]
- convergence excess [SNOMED Notion]
- convergence insufficiency [SNOMED Notion]
- cyclophoria [SNOMED Notion]
- eye movement disorders [MedlinePlus Topic]
- internuclear ophthalmoplegia [DO Concept]
- internuclear ophthalmoplegia [SNOMED Notion]
- ocular motility disease [DO Concept]
- ophthalmoplegia, nos [SNOMED Notion]
- opsoclonus [SNOMED Notion]
- parinaud's syndrome [SNOMED Notion]
- paroxysmal ocular dyskinesia [SNOMED Notion]
- pseudoophthalmoplegia [SNOMED Notion]
- skew deviation [SNOMED Notion]
DO Cross reference
- Brown's tendon sheath syndrome [DO Concept]
- internuclear ophthalmoplegia [DO Concept]
- ocular motility disease [DO Concept]
HPO term
- Impaired convergence [HPO term]
- Internuclear ophthalmoplegia [HPO term]
- Opsoclonus [HPO term]
Record concept(s)
- brown tendon sheath syndrome [MeSH concept]
- convergence excess [MeSH concept]
- convergence insufficiency [MeSH concept]
- cyclophoria [MeSH concept]
- internuclear ophthalmoplegia [MeSH concept]
- ocular motility disorders [MeSH concept]
- ocular torticollis [MeSH concept]
- opsoclonus [MeSH concept]
- parinaud syndrome [MeSH concept]
- paroxysmal ocular dyskinesia [MeSH concept]
- pseudoophthalmoplegia [MeSH concept]
- skew deviation [MeSH concept]
- smooth pursuit deficiency [MeSH concept]
- spasm of conjugate gaze [MeSH concept]
Related MeSH Supplementary Concept(s)
- Levator-Medial rectus synkinesis [MeSH Supplementary Concept]
- Setting-Sun phenomenon, familial benign [MeSH Supplementary Concept]
- athabaskan brainstem dysgenesis [MeSH Supplementary Concept]
- cyclotropia [MeSH Supplementary Concept]
- diffuse lewy body disease with gaze palsy [MeSH Supplementary Concept]
- fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement [MeSH Supplementary Concept]
- fibrosis of extraocular muscles, congenital, 3B [MeSH Supplementary Concept]
- fibrosis of extraocular muscles, congenital, 3C [MeSH Supplementary Concept]
- fibrosis of extraocular muscles, congenital, with synergistic divergence [MeSH Supplementary Concept]
- joubert syndrome 3 [MeSH Supplementary Concept]
- joubert syndrome 5 [MeSH Supplementary Concept]
- joubert syndrome 6 [MeSH Supplementary Concept]
- joubert syndrome 7 [MeSH Supplementary Concept]
- mental retardation, X-Linked, syndromic, christianson type [MeSH Supplementary Concept]
- paroxysmal tonic upgaze, benign childhood, with ataxia [MeSH Supplementary Concept]
- tukel syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder of eye movements (disorder) [SNOMED CT concept]
- Eye movement disorder [MedDRA Preferred Term]
- Eye movement disorder NOS [MedDRA LLT]
- Eye movement disorders [MedDRA High Level Term]
- Ocular motility disorder [PASCAL descriptor]
- Unspecified disorder of eye movements [ICD-9 code]
- disorder of eye movements, nos [SNOMED Notion]
- eye movement disorders [MedlinePlus Topic]
- ocular motility disease [DO Concept]
- ocular motility disorder [Disease (Nov.)]
Validated automatic mappings to BTNT
- Brown syndrome [Disease (Nov.)]
- Brown's tendon sheath syndrome [DO Concept]
- Brown's tendon sheath syndrome (disorder) [SNOMED CT concept]
- Parinaud syndrome [Disease (Nov.)]
- convergence excess [Disease (Nov.)]
- convergence insufficiency [Disease (Nov.)]
- internuclear ophthalmoplegia [Disease (Nov.)]
- opsoclonus [Disease (Nov.)]
- paroxysmal ocular dyskinesia [Disease (Nov.)]
- pseudoophthalmoplegia [Disease (Nov.)]
- smooth pursuit deficiency [Disease (Nov.)]

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