You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Neuronopathy, distal hereditary motor, autosomal recessive 5, look for clinical trials, and connect with others living with it — all in one place.
Open the full Neuronopathy, distal hereditary motor, autosomal recessive 5 hub →Neuronopathy, distal hereditary motor, autosomal recessive 5 is a rare condition. Also known as Autosomal recessive distal spinal muscular atrophy type 5, Young adult-onset dHMN, dSMA5. Tomeko brings together the specialists, research, clinical trials, treatments and community for Neuronopathy, distal hereditary motor, autosomal recessive 5 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:314485 · OMIM 614881, 619216 · ICD-10 G12.2 · GARD 0017421
Start by learning the basics from an authoritative source, find a specialist or center that sees Neuronopathy, distal hereditary motor, autosomal recessive 5, 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 recessive 5, filtered to your area.
Tomeko shows live, recruiting studies for Neuronopathy, distal hereditary motor, autosomal recessive 5 from ClinicalTrials.gov on the hub.