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GENATLAS PHENOTYPE

last update : 18-10-2018

Symbol	SCAR25
Location	6q21
Name	spinocerebellar ataxia, autosomal recessive 25
Corresponding gene	ATG5
Main clinical features	delayed psychomotor development with delayed walking, truncal ataxia, dysmetria, nystagmus, and low IQ (68 and 70); brain imaging showed cerebellar hypoplasia
Genetic determination	autosomal recessive
Function/system disorder	neurology
Type	disease

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