You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary spastic paraplegia 39, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary spastic paraplegia 39 hub →Hereditary spastic paraplegia 39 is a rare condition. Also known as SPG39, Spastic paraplegia due to NTE mutation, Spastic paraplegia due to neuropathy target esterase mutation. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary spastic paraplegia 39 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:139480 · OMIM 612020 · ICD-10 G11.4 · GARD 0004924
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary spastic paraplegia 39, 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 spastic paraplegia 39, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary spastic paraplegia 39 from ClinicalTrials.gov on the hub.