You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Charcot-Marie-Tooth disease, demyelinating, type 1G, look for clinical trials, and connect with others living with it — all in one place.
Open the full Charcot-Marie-Tooth disease, demyelinating, type 1G hub →Charcot-Marie-Tooth disease, demyelinating, type 1G is a rare condition. Also known as PMP2-related CMT1, PMP2-related Charcot-Marie-Tooth neuropathy type 1, PMP2-related hereditary motor and sensory neuropathy type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Charcot-Marie-Tooth disease, demyelinating, type 1G so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:476394 · OMIM 618279 · ICD-10 G60.0 · GARD 0017851
Start by learning the basics from an authoritative source, find a specialist or center that sees Charcot-Marie-Tooth disease, demyelinating, type 1G, 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 Charcot-Marie-Tooth disease, demyelinating, type 1G, filtered to your area.
Tomeko shows live, recruiting studies for Charcot-Marie-Tooth disease, demyelinating, type 1G from ClinicalTrials.gov on the hub.