You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Neuronopathy, distal hereditary motor, autosomal dominant 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Neuronopathy, distal hereditary motor, autosomal dominant 1 hub →Neuronopathy, distal hereditary motor, autosomal dominant 1 is a rare condition. Also known as Autosomal dominant distal juvenile spinal muscular atrophy type 1, dHMN1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Neuronopathy, distal hereditary motor, autosomal dominant 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:139518 · OMIM 182960 · ICD-10 G12.2 · GARD 0016953
Start by learning the basics from an authoritative source, find a specialist or center that sees Neuronopathy, distal hereditary motor, autosomal dominant 1, 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 Neuronopathy, distal hereditary motor, autosomal dominant 1, filtered to your area.
Tomeko shows live, recruiting studies for Neuronopathy, distal hereditary motor, autosomal dominant 1 from ClinicalTrials.gov on the hub.