You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary sensory and autonomic neuropathy type 7, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary sensory and autonomic neuropathy type 7 hub →Hereditary sensory and autonomic neuropathy type 7 is a rare condition. Also known as CIP with hyperhidrosis and gastrointestinal dysfunction, Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction, HSAN with hyperhidrosis and gastrointestinal dysfunction, HSAN7, Hereditary sensory and autonomic neuropathy type VII, Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary sensory and autonomic neuropathy type 7 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:391397 · OMIM 615548 · ICD-10 G60.8 · GARD 0012732
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary sensory and autonomic neuropathy type 7, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary sensory and autonomic neuropathy type 7, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary sensory and autonomic neuropathy type 7 from ClinicalTrials.gov on the hub.