Related MeSH Hierarchy (4)
Diseases [C] » Musculoskeletal Diseases [C05] » Muscular Diseases » Muscular Disorders, Atrophic » Muscular Dystrophies » Muscular Dystrophy, Emery-Dreifuss » X-Linked Emery-Dreifuss Muscular Dystrophy
Diseases [C] » Nervous System Diseases [C10] » Neuromuscular Diseases » Muscular Diseases » Muscular Disorders, Atrophic » Muscular Dystrophies » Muscular Dystrophy, Emery-Dreifuss » X-Linked Emery-Dreifuss Muscular Dystrophy
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Muscular Dystrophy, Emery-Dreifuss » X-Linked Emery-Dreifuss Muscular Dystrophy
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Muscular Dystrophies » Muscular Dystrophy, Emery-Dreifuss » X-Linked Emery-Dreifuss Muscular Dystrophy
Description
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. MeSH
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