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Autosomal recessive syndromic cerebellar ataxia

rare
Identifiers
MONDO:0020047 Orphanet:98099
Part of
Autosomal recessive cerebellar ataxia

Subtypes

All diseases Rare only
Disease Subtypes
Gemignani syndrome
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Ataxia - oculomotor apraxia type 4
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
Autosomal recessive spinocerebellar ataxia 11
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
Peroxisome biogenesis disorder 4B

Rare disease

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