You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6), look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) hub →Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) is a rare condition. Also known as Autosomal dominant limb-girdle muscular dystrophy type 1D, DNAJB6-related LGMD D1, LGMD type 1D, LGMD1D, Limb-girdle muscular dystrophy type 1D. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:34516 · OMIM 603511 · ICD-10 G71.0 · GARD 0012528
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6), 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 Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6), filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) from ClinicalTrials.gov on the hub.