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abetalipoproteinemia
MONDO:0008692
cerebrotendinous xanthomatosis
MONDO:0008948
familial isolated deficiency of vitamin E
MONDO:0010188
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
MONDO:0011835
autosomal recessive ataxia due to PEX10 deficiency
MONDO:0016614
autosomal recessive cerebellar ataxia with late-onset spasticity
MONDO:0018129