Impaired smooth pursuit

Symptom Information:

Symptom ID: HPO:0007772
Synonyms:
Abnormal visual pursuit [HPO:0007772]
Abnormal visual pursuit [OMIM:Abnormal visual pursuit]
Impaired smooth pursuit [OMIM:Impaired smooth pursuit]
Quality:
Cross references:
OMIM: "Abnormal visual pursuit" [OMIM:Abnormal visual pursuit]
OMIM: "Impaired smooth pursuit" [OMIM:Impaired smooth pursuit]
Is a (Direct Parents):
HPO         Abnormality of ocular smooth pursuit
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)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Alpha-mannosidosis (Orphanet:61)
Ataxia-telangiectasia-like disorder (Orphanet:251347)
Autosomal recessive cerebellar ataxia - psychomotor retardation (Orphanet:284271)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 2 (OMIM:608091)
Leber congenital amaurosis 15 (OMIM:613843)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
PEROXISOME BIOGENESIS DISORDER 6B (OMIM:614871)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
Pontocerebellar hypoplasia type 2 (Orphanet:2524)
Spinocerebellar ataxia type 15/16 (Orphanet:98769)
Spinocerebellar ataxia type 27 (Orphanet:98764)
Spinocerebellar ataxia type 36 (Orphanet:276198)
Spinocerebellar ataxia type 4 (Orphanet:98765)
Spinocerebellar ataxia type 5 (Orphanet:98766)
Spinocerebellar ataxia type 6 (Orphanet:98758)
Spinocerebellar ataxia type 8 (Orphanet:98760)