You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome hub →Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome is a rare condition. Also known as HIBM3, Hereditary inclusion body myopathy type 3, IBM3, Inclusion body myopathy type 3. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79091 · OMIM 605637 · ICD-10 G71.8 · GARD 0009494
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome, 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 inclusion body myopathy-joint contractures-ophthalmoplegia syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome from ClinicalTrials.gov on the hub.