Gaze-evoked nystagmus
Symptom Information:
Symptom ID: | HPO:0000640 | ||||
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) Abnormal involuntary eye movements(HPO:0012547) Nystagmus(HPO:0000639) Gaze-evoked nystagmus(HPO:0000640) MedDRA: |
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Database Frequency: | 27 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit | (Orphanet:284282) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 | (OMIM:224050) |
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA | (OMIM:614306) |
Dysequilibrium syndrome | (Orphanet:1766) |
Episodic ataxia type 4 | (Orphanet:79136) |
Episodic ataxia type 5 | (Orphanet:211067) |
Familial paroxysmal ataxia | (Orphanet:97) |
Leber plus disease | (Orphanet:99718) |
Multiple system atrophy | (Orphanet:102) |
NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT | (OMIM:193003) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Perrault Syndrome 5 | (OMIM:616138) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 27 | (Orphanet:98764) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 30 | (Orphanet:211017) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |
Spinocerebellar ataxia type 6 | (Orphanet:98758) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |