Impaired horizontal smooth pursuit
Symptom Information:
Symptom ID: | HPO:0001151 | |||
Synonyms: |
|
|||
Quality: | ||||
Cross references: |
|
|||
Is a (Direct Parents): |
|
|||
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) Impaired smooth pursuit(HPO:0007772) Impaired horizontal smooth pursuit(HPO:0001151) MedDRA: |
|||
Database Frequency: | 7 / 7739 | |||
Resource: |
All diseases associated with this symptom:
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 26 | (Orphanet:101112) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |