Phenotypes for disease #01564 (SCA6 (ataxia, spinocerebellar, type 6), OMIM:183086)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000245126 (+) Astigmatism,(+) Ataxia,(+) Short stature,(+) Downbeat nystagmus - - Unknown 02y - - - - Andreas Laner 00326660
0000254876 clinical suspicion of SCA; (+) Abnormality of the philtrum,(+) Broad philtrum,(+) Muscle weakness,(+) Aplasia/Hypoplasia of fingers,(+) Abnormal ear morphology - - Unknown 00y06m - - - - Andreas Laner 00359604
0000257412 Progressive ataxia from 30 years of age (possible childhood onset) associated with myoclonus, on a background of mild intellectual impairment and sensorineural hearing impairment. MRI showing cerebellar atrophy and EEG findings of diffuse paroxysmal abnormalities consistent with encephalopathy. No migraine. Family history of epilepsy and possible ataxia affecting father and brother (now deceased). late onset progressive myoclonus epilepsy - Familial, autosomal dominant - - - - - Johan den Dunnen 00334917
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