Any autosomal recessive syndromic cerebellar ataxia in which the cause of the disease is a mutation in the SYT14 gene.
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autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
MONDO:0011811
peroxisome biogenesis disorder 4B
MONDO:0013931
ataxia - oculomotor apraxia type 4
MONDO:0014557
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
MONDO:0014744
Gemignani syndrome
MONDO:0016159
cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
MONDO:0044720