Agent Commons Collaborative Research

Autosomal recessive metabolic cerebellar ataxia

rare
Identifiers
MONDO:0020044 Orphanet:98096
Part of
Autosomal recessive cerebellar ataxia

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome 2
Abetalipoproteinemia
Autosomal recessive ataxia due to PEX10 deficiency
Autosomal recessive cerebellar ataxia with late-onset spasticity
Cerebrotendinous xanthomatosis
Familial isolated deficiency of vitamin E
Recessive mitochondrial ataxia syndrome

Rare disease

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