Emery-Dreifuss muscular dystrophy associated with mutations on emerin (EMD gene) or four and a half LIM domains 1 (FHL1 gene) both located on X chromosome.
Also Known As:
Benign Scapuloperoneal Muscular Dystrophy with Early Contractures; Emery-Dreifuss Muscular Dystrophy 6; Emery-Dreifuss Muscular Dystrophy 6, X-Linked; Emery-Dreifuss Muscular Dystrophy, 1; Emery-Dreifuss Muscular Dystrophy, X-Linked; Myopathy, X-Linked, With Postural Muscle Atrophy; Scapuloperoneal Syndrome, X-Linked; Emerinopathies; Emery Dreifuss Muscular Dystrophy 1; Emery Dreifuss Muscular Dystrophy 1, X Linked; Emery Dreifuss Muscular Dystrophy 6; Emery Dreifuss Muscular Dystrophy 6, X Linked; Emery Dreifuss Muscular Dystrophy, 1; Emery Dreifuss Muscular Dystrophy, X Linked; Scapuloperoneal Syndrome, X Linked; X Linked Emery Dreifuss Muscular Dystrophy; X-Linked Scapuloperoneal Syndrome; EDMD1; Emerinopathy; Emery-Dreifuss Muscular Dystrophy 1; Emery-Dreifuss Muscular Dystrophy 1, X-Linked; Muscular Dystrophy, Emery-Dreifuss, X-Linked; XMPMA