Abnormality of eye movement

Symptom Information:

Symptom ID: HPO:0000496
Synonyms:
Abnormal extraocular movement [HPO:0000496]
Abnormal extraocular movements [HPO:0000496]
Abnormal eye motility [HPO:0000496]
Abnormal eye movement [HPO:0000496]
Abnormal eye movements [HPO:0000496]
Abnormal ocular movements [HPO:0000496]
Eye movement abnormalities [HPO:0000496]
Ocular movement abnormalities [HPO:0000496]
Oculomotor abnormalities [HPO:0000496]
Eye movements anomaly [Orphanet:5840]
Abnormal ocular motility (finding) [Orphanet:5840]
Abnormal ocular motility [Orphanet:5840]
Abnormal extraocular movement [OMIM:Abnormal extraocular movement]
Abnormal extraocular movements [OMIM:Abnormal extraocular movements]
Abnormal eye motility [OMIM:Abnormal eye motility]
Abnormal eye movement [OMIM:Abnormal eye movement]
Abnormal eye movements [OMIM:Abnormal eye movements]
Abnormal ocular movements [OMIM:Abnormal ocular movements]
Eye movement abnormalities [OMIM:Eye movement abnormalities]
Ocular movement abnormalities [OMIM:Ocular movement abnormalities]
Oculomotor abnormalities [OMIM:Oculomotor abnormalities]
Abnormal eye movements/oculomotor disorder [Orphanet:5840]
Abnormal eye movements NOS [Orphanet:5840]
Eye movement disorder [MedDRA:10061129]
Abnormal eye movements NOS [MedDRA:10061129]
Deficiencies of saccadic eye movements [MedDRA:10061129]
Deficiencies of smooth pursuit movements [MedDRA:10061129]
Eye movement disorder NOS [MedDRA:10061129]
Eye rolling [MedDRA:10061129]
Eyes rolling [MedDRA:10061129]
Other irregularities of eye movements [MedDRA:10061129]
Unspecified disorder of eye movements [MedDRA:10061129]
Ocular deviation [MedDRA:10061129]
Abnormal eye movements (in some patients) [OMIM:Abnormal eye movements (in some patients)]
Eye movement disorder [OMIM:Eye movement disorder]
Eye movement disorders [MedDRA:10015951]
Quality:
Cross references:
HPO:0000570 "Abnormality of saccadic eye movements" [Orphanet:5840]
Orphanet:5840 "Abnormal eye movements/oculomotor disorder" [Orphanet:5840]
OMIM: "Abnormal extraocular movement" [OMIM:Abnormal extraocular movement]
OMIM: "Abnormal extraocular movements" [OMIM:Abnormal extraocular movements]
OMIM: "Abnormal eye motility" [OMIM:Abnormal eye motility]
OMIM: "Abnormal eye movement" [OMIM:Abnormal eye movement]
OMIM: "Abnormal eye movements" [OMIM:Abnormal eye movements]
OMIM: "Abnormal ocular movements" [OMIM:Abnormal ocular movements]
OMIM: "Eye movement abnormalities" [OMIM:Eye movement abnormalities]
OMIM: "Ocular movement abnormalities" [OMIM:Ocular movement abnormalities]
OMIM: "Oculomotor abnormalities" [OMIM:Oculomotor abnormalities]
OMIM: "Abnormal eye movements (in some patients)" [OMIM:Abnormal eye movements (in some patients)]
OMIM: "Eye movement disorder" [OMIM:Eye movement disorder]
UMLS:C0497202 "Abnormal ocular motility" [Orphanet:5840]
Is a (Direct Parents):
MedDRA Cranial nerve disorders (excl neoplasms)
MedDRA Ocular nerve and muscle disorders
HPO         Abnormal eye physiology
Orphanet Abnormality of the eye
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of eye movement(HPO:0000496)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Cranial nerve disorders (excl neoplasms)(MedDRA:10011305)
       Abnormality of eye movement(HPO:0000496)
Eye disorders(MedDRA:10015919)
    Ocular neuromuscular disorders(MedDRA:10030061)
       Ocular nerve and muscle disorders(MedDRA:10030059)
          Abnormality of eye movement(HPO:0000496)
Database Frequency: 79 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 1 (OMIM:257920)
4-hydroxybutyric aciduria (Orphanet:22)
AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
AICARDI-GOUTIERES SYNDROME 7 (OMIM:615846)
ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 (OMIM:104290)
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 (OMIM:614820)
ARIMA SYNDROME (OMIM:243910)
ATAXIA-TELANGIECTASIA (OMIM:208900)
Alexander disease (Orphanet:58)
Ataxia-telangiectasia (Orphanet:100)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Bardet-Biedl syndrome 7 (OMIM:615984)
Benign paroxysmal tonic upgaze of childhood with ataxia (Orphanet:1179)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
Blue diaper syndrome (Orphanet:94086)
Bosley-Salih-Alorainy syndrome (Orphanet:69737)
CEDNIK syndrome (Orphanet:66631)
Choreoacanthocytosis (Orphanet:2388)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Dihydropyrimidine dehydrogenase deficiency (Orphanet:1675)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Duane anomaly - myopathy - scoliosis (Orphanet:50817)
Duane retraction syndrome (Orphanet:233)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Fetal Gaucher disease (Orphanet:85212)
Friedreich ataxia 1 (OMIM:229300)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease (Orphanet:355)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
Hermansky-Pudlak syndrome (Orphanet:79430)
Huntington disease (Orphanet:399)
Hurler syndrome (Orphanet:93473)
Infantile dystonia-parkinsonism (Orphanet:238455)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Infantile-onset ascending hereditary spastic paralysis (Orphanet:293168)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Isolated cerebellar hypoplasia/agenesis (Orphanet:1398)
Isolated plagiocephaly (Orphanet:35098)
Joubert syndrome 18 (OMIM:614815)
Joubert syndrome 3 (OMIM:608629)
Joubert syndrome 4 (OMIM:609583)
Joubert syndrome 6 (OMIM:610688)
Juvenile Huntington disease (Orphanet:248111)
KURU, SUSCEPTIBILITY TO (OMIM:245300)
LEBER OPTIC ATROPHY AND DYSTONIA (OMIM:500001)
Leigh syndrome (Orphanet:506)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Narcolepsy-cataplexy (Orphanet:2073)
Neuroferritinopathy (Orphanet:157846)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 4 (Orphanet:2753)
PEHO syndrome (Orphanet:2836)
PMM2-CDG (Orphanet:79318)
Perrault Syndrome 5 (OMIM:616138)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pontine tegmental cap dysplasia (Orphanet:269229)
Primary basilar impression (Orphanet:2285)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Refsum disease (Orphanet:773)
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION (OMIM:607565)
Spectrin-associated autosomal recessive cerebellar ataxia (Orphanet:352403)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 14 (Orphanet:98763)
Spinocerebellar ataxia type 26 (Orphanet:101112)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Wyburn-Mason syndrome (Orphanet:53719)
X-linked retinoschisis (Orphanet:792)