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 acrodystrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary motor and sensory neuropathy with acrodystrophy hub →Hereditary motor and sensory neuropathy with acrodystrophy is a rare condition. Also known as AR-CMT2 with acrodystrophy, Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy, Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy, HMSN with acrodystrophy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary motor and sensory neuropathy with acrodystrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:90119 · ICD-10 G60.0 · GARD 0019124
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary motor and sensory neuropathy with acrodystrophy, 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 acrodystrophy, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary motor and sensory neuropathy with acrodystrophy from ClinicalTrials.gov on the hub.