Slow saccadic eye movements

Symptom Information:

Symptom ID: HPO:0000514
Synonyms:
Slow saccades [HPO:0000514]
Slow saccades [OMIM:Slow saccades]
Slow saccades (less common) [OMIM:Slow saccades (less common)]
Slow saccades (with longer disease duration) [OMIM:Slow saccades (with longer disease duration)]
Quality:
Cross references:
OMIM: "Slow saccades" [OMIM:Slow saccades]
OMIM: "Slow saccades (less common)" [OMIM:Slow saccades (less common)]
OMIM: "Slow saccades (with longer disease duration)" [OMIM:Slow saccades (with longer disease duration)]
Is a (Direct Parents):
HPO         Abnormality of saccadic eye movements
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 saccadic eye movements(HPO:0000570)
                   Slow saccadic eye movements(HPO:0000514)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-OCULOMOTOR APRAXIA 3 (OMIM:615217)
Autosomal dominant spastic ataxia 1 (Orphanet:251282)
Autosomal recessive spastic paraplegia type 44 (Orphanet:320401)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Huntington disease (Orphanet:399)
Kufor-Rakeb syndrome (Orphanet:306674)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:260300)
PEROXISOME BIOGENESIS DISORDER 5B (OMIM:614867)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
SPINOCEREBELLAR ATAXIA 38 (OMIM:615957)
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS (OMIM:271322)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Spinocerebellar ataxia type 23 (Orphanet:101108)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Spinocerebellar ataxia type 36 (Orphanet:276198)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Spinocerebellar ataxia type 8 (Orphanet:98760)
X-linked progressive cerebellar ataxia (Orphanet:1175)