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:468666
isolated anhidrosis with normal sweat glands
OrphanetORPHA:468666
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
isolated anhidrosis with normal sweat glands | OrphanDrug