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References OMIM Gene GeneReviews HGMD HGNC
last update : 04-04-2012
Symbol SNAX1
Location 8p11.21
HGNC id 23701
Name sensory ataxia 1
Corresponding gene RNF170
Other symbol(s) ADSA
Main clinical features
  • adulthood onset, variable pyramidal weakness, involvement of preganglionic sensory nerve fibers, loss of sensation and reflexes in the limbs and a delay in somatosensory evoked potentials but with nerve conduction and biposy normal
  • Genetic determination autosomal dominant
    Function/system disorder neurology
    Type disease