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Up to: Syndromic disease · Acute disease · Autosomal recessive syndromic cerebellar ataxia
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
An autosomal recessive cerebellar ataxia that has material basis in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.
This condition has no sub-types.