x

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Hereditary sensory and autonomic neuropathy type 2

Disease definition

Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an inherited disorder characterized by profound and universal sensory loss involving large and small fiber nerves, and marked hypotonia.

ORPHA:970

  • Synonym(s):
    • Autosomal recessive sensory radicular neuropathy
    • HSAN2
    • Hereditary sensory and autonomic neuropathy type II
    • Neurogenic acroosteolysis
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: G60.8
  • OMIM: 201300  243000  613115  614213
  • UMLS: C0020072  C0270914
  • MeSH: -
  • GARD: 3976
  • MedDRA: -

Detailed information

Professionals

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.