Phenotypes for disease #04243 (SCAR17 (ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17)), OMIM:616127)

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

Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

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Individual ID     
0000028247 - - - Familial, autosomal recessive - - - - - Mike Gerards 00037591
0000028259 see paper; hypotonia, developmental delay, mental retardation, non- progressive truncal and extremity ataxia; MRI demonstrated hypoplasia vermis and cerebellar hemispheres; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00037743
0000304778 Global developmental delay, Cerebellar hypoplasia, Dandy-Walker malformation, Hypoplasia of the corpus callosum, Aplasia/Hypoplasia involving the central nervous system, Intellectual disability, Poor fine motor coordination, Delayed gross motor development, Facial grimacing, Bradyphrenia, Behavioral abnormality, Attention deficit hyperactivity disorder - - Familial, autosomal recessive 10y - - - - Andreas Laner 00412787
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