Autosomal recessive metabolic cerebellar ataxia
MONDO:002004438 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Cerebrotendinous xanthomatosis
(6)
Abetalipoproteinemia
(2)
Familial isolated deficiency of vitamin E
(1)
Recessive mitochondrial ataxia syndrome
(1)
Autosomal recessive ataxia due to PEX10 deficiency
(0)
Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
(0)
Autosomal recessive cerebellar ataxia with late-onset spasticity
(0)
Autosomal recessive spinocerebellar ataxia 13
(0)
Autosomal recessive spinocerebellar ataxia 18
(0)