hereditary sensory neuropathy type 1B
MeSH: C564296ORPHA: 139564
Overview
hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has material basis in variation in the chromosome region 3p24-p22
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C564296Orphanet Code
ORPHA:139564hereditary sensory neuropathy type 1B
| MeSH | C564296 |
| Orphanet | ORPHA:139564 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO