Abnormality of eye movement
Symptom Information:
Symptom ID: | HPO:0000496 | ||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |