isolated anhidrosis with normal sweat glands
ORPHA: 468666
Overview
anhidrosis that has material basis in homozygous mutation in the ITPR2 gene on chromosome 12p11
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:468666isolated anhidrosis with normal sweat glands
| Orphanet | ORPHA:468666 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO