Impaired smooth pursuit
Symptom Information:
Symptom ID: | HPO:0007772 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |