Hypometric saccades
Symptom Information:
Symptom ID: | HPO:0000571 | ||||
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 saccadic eye movements(HPO:0000570) Hypometric saccades(HPO:0000571) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome | (Orphanet:363429) |
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency | (Orphanet:324262) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Joubert syndrome 4 | (OMIM:609583) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Spectrin-associated autosomal recessive cerebellar ataxia | (Orphanet:352403) |