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Autosomal recessive ataxia due to ubiquinone deficiency
What is Autosomal recessive ataxia due to ubiquinone deficiency?
This syndrome is characterised by childhood-onset progressive ataxia and cerebellar atrophy.
Other condition names
ARCA2
Autosomal recessive ataxia due to coenzyme Q10 deficiency
Autosomal recessive cerebellar ataxia type 2
Autosomal recessive spinocerebellar ataxia type 9
SCAR9
Inheritance type
Autosomal recessive
Prevalence
Worldwide: <1 in 1,000 000
Age of Onset
Childhood
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.