Autosomal recessive ataxia due to ubiquinone deficiency

MONDO:0012784

This syndrome is characterized by childhood-onset progressive ataxia and cerebellar atrophy.

Also known as: ARCA2, SCAR9, autosomal recessive ataxia due to coenzyme Q10 deficiency, autosomal recessive cerebellar ataxia type 2, autosomal recessive spinocerebellar ataxia type 9, coenzyme Q10 deficiency, primary, type 4, COQ10D4, autosomal recessive spinocerebellar ataxia 9

37 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive ataxia due to ubiquinone deficiency itself.

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↑ Autosomal recessive cerebellar ataxia (72) ↑ Coenzyme Q10 deficiency (3)

Including sub-types (37) Tagged with Autosomal recessive ataxia due to ubiquinone deficiency (0)

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