Gaze-evoked nystagmus

Symptom Information:

Symptom ID: HPO:0000640
Synonyms:
Gaze-evoked nystagmus [OMIM:Gaze-evoked nystagmus]
Gaze-evoked nystagmus (1 patient) [OMIM:Gaze-evoked nystagmus (1 patient)]
Gaze-evoked nystagmus (33%) [OMIM:Gaze-evoked nystagmus (33%)]
Nystagmus, gaze-evoked [OMIM:Nystagmus, gaze-evoked]
Quality:
Cross references:
OMIM: "Gaze-evoked nystagmus" [OMIM:Gaze-evoked nystagmus]
OMIM: "Gaze-evoked nystagmus (1 patient)" [OMIM:Gaze-evoked nystagmus (1 patient)]
OMIM: "Gaze-evoked nystagmus (33%)" [OMIM:Gaze-evoked nystagmus (33%)]
OMIM: "Nystagmus, gaze-evoked" [OMIM:Nystagmus, gaze-evoked]
Is a (Direct Parents):
HPO         Nystagmus
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:
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)