You are not alone. Here is where to start: learn the basics, find a specialist or center that sees X-linked distal spinal muscular atrophy type 3, look for clinical trials, and connect with others living with it — all in one place.
Open the full X-linked distal spinal muscular atrophy type 3 hub →X-linked distal spinal muscular atrophy type 3 is a rare condition. Also known as ATP7A-related distal motor neuropathy, DSMAX, SMAX3, X-linked dHMN3, X-linked dSMA3, X-linked distal hereditary motor neuropathy type 3. Tomeko brings together the specialists, research, clinical trials, treatments and community for X-linked distal spinal muscular atrophy type 3 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:139557 · OMIM 300489 · ICD-10 G12.1 · GARD 0016957
Start by learning the basics from an authoritative source, find a specialist or center that sees X-linked distal spinal muscular atrophy type 3, 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 X-linked distal spinal muscular atrophy type 3, filtered to your area.
Tomeko shows live, recruiting studies for X-linked distal spinal muscular atrophy type 3 from ClinicalTrials.gov on the hub.