Concept: dm
Label (en): myotonic dystrophy
Description (en): long term genetic disorder that affects muscle function
Also known as (en): Dystrophia myotonica, Steinert disease, congenital myotonic dystrophy, myotonic dystrophy of Steinert, Myotonic dystrophy type 1, MYOTONIC DYSTROPHY 1, MYOTONIC DYSTROPHY 1; DM1, DM1, MD1, Steinert myotonic dystrophy, Dystrophia Myotonica 1
Label (es): distrofia miotónica de Steinert
Description (es): enfermedad hereditaria autosómica dominante
Also known as (es): Distrofia miotonica de Steinert, Distrofia muscular miotónica, Distrofia miotónica, Distrofia miotonica, Distrofia muscular miotonica, distrofia miotónica de tipo 1, Distrofia miotónica, tipo 1, Distrofia miotonica, tipo 1, Distrofia miotonica tipo 1, Distrofia miotónica tipo 1, enfermedad de Steinert, DM1
Label (ca): distròfia miotònica de Steinert
Description (ca): malaltia hereditària autosòmica dominant
Label (it): distrofia miotonica
Instance of: rare disease, class of disease
Subclass of: myotonic disease, hypertrophic cardiomyopathy, organic brain syndrome, ptosis, myopathy with eye involvement, syndrome associated with hypertrophic cardiomyopathy, musculoskeletal disease with cataract, hypergonadotropic hypogonadism, disease