hereditary sensory and autonomic neuropathy type 2
ORPHA: 970
Overview
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
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary sensory and autonomic neuropathy type 2, sourced from HPO and Orphanet clinical annotations.
HyperhidrosisTapered fingerDystrophic toenailFoot acroosteolysisWormian bonesOsteolysisAbnormality of the kneeAbnormality of the ankleAbnormal cortical bone morphologySkeletal muscle atrophyAbnormal hip bone morphologyHyperlordosisReduced bone mineral densityAbnormal epiphysis morphologyDystrophic fingernails
Classification & Codes
Orphanet Code
ORPHA:970hereditary sensory and autonomic neuropathy type 2
| Orphanet | ORPHA:970 |
| Treatments | 0 drug(s) |
| Symptoms on record | 15 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO