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References OMIM Gene GeneReviews HGMD HGNC
last update : 10/07/2006
Symbol HSAN5
Location 1p13.2-p11.2
Name hereditary sensory and autonomic neuropathy, type V
Other name(s) insensitivity to pain, congenital
Corresponding gene NGF
Main clinical features
  • pain insensitivity (loss of deep pain perception, from bone fractures and joints and heat perception)
  • Genetic determination autosomal recessive
    Function/system disorder neurology
    Type disease
    Gene product
    Name nerve growth factor