Abnormality of ocular smooth pursuit

Symptom Information:

Symptom ID: HPO:0000617
Synonyms:
Abnormal smooth pursuits [HPO:0000617]
Disrupted ocular pursuit movements [HPO:0000617]
Impaired smooth pursuit ocular movements [HPO:0000617]
Irregular visual pursuit movements [HPO:0000617]
Abnormal smooth pursuits [OMIM:Abnormal smooth pursuits]
Disrupted ocular pursuit movements [OMIM:Disrupted ocular pursuit movements]
Impaired smooth pursuit ocular movements [OMIM:Impaired smooth pursuit ocular movements]
Irregular visual pursuit movements [OMIM:Irregular visual pursuit movements]
Abnormal smooth pursuit [OMIM:Abnormal smooth pursuit]
Quality:
Cross references:
OMIM: "Abnormal smooth pursuits" [OMIM:Abnormal smooth pursuits]
OMIM: "Disrupted ocular pursuit movements" [OMIM:Disrupted ocular pursuit movements]
OMIM: "Impaired smooth pursuit ocular movements" [OMIM:Impaired smooth pursuit ocular movements]
OMIM: "Irregular visual pursuit movements" [OMIM:Irregular visual pursuit movements]
OMIM: "Abnormal smooth pursuit" [OMIM:Abnormal smooth pursuit]
Is a (Direct Parents):
HPO         Abnormality of eye movement
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)
                Abnormality of ocular smooth pursuit(HPO:0000617)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Alpha-mannosidosis (Orphanet:61)
Episodic ataxia type 4 (Orphanet:79136)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
Odontoleukodystrophy (Orphanet:77295)
Spinocerebellar ataxia type 26 (Orphanet:101112)
Spinocerebellar ataxia type 27 (Orphanet:98764)