You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary motor and sensory neuropathy with optic atrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary motor and sensory neuropathy with optic atrophy hub →Hereditary motor and sensory neuropathy with optic atrophy is a rare condition. Also known as CMT6, Charcot-Marie-Tooth disease type 6, HMSN 6, HMSN VI, Hereditary motor and sensory neuropathy type VI, Peripheral neuropathy and optic atrophy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary motor and sensory neuropathy with optic atrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:90120 · OMIM 601152, 616505 · ICD-10 G60.0 · GARD 0016787
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary motor and sensory neuropathy with optic atrophy, 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 motor and sensory neuropathy with optic atrophy, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary motor and sensory neuropathy with optic atrophy from ClinicalTrials.gov on the hub.