(Q50349727)

English

hereditary sensory and autonomic neuropathy type 2

hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood

  • HSAN2
  • hereditary sensory and autonomic neuropathy type II
  • Autosomal recessive sensory radicular neuropathy
  • Neurogenic acroosteolysis

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