You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Charcot-Marie-Tooth disease axonal type 2X, look for clinical trials, and connect with others living with it — all in one place.
Open the full Charcot-Marie-Tooth disease axonal type 2X hub →Charcot-Marie-Tooth disease axonal type 2X is a rare condition. Also known as Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation, CMT2X, ARCMT2X. Tomeko brings together the specialists, research, clinical trials, treatments and community for Charcot-Marie-Tooth disease axonal type 2X so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:466775 · OMIM 616668 · ICD-10 G60.0 · GARD 0017830
Start by learning the basics from an authoritative source, find a specialist or center that sees Charcot-Marie-Tooth disease axonal type 2X, 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 axonal type 2X, filtered to your area.
Tomeko shows live, recruiting studies for Charcot-Marie-Tooth disease axonal type 2X from ClinicalTrials.gov on the hub.