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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Muscular Dystrophy, Emery-Dreifuss > X-Linked Emery-Dreifuss Muscular Dystrophy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Muscular Dystrophies > Muscular Dystrophy, Emery-Dreifuss > X-Linked Emery-Dreifuss Muscular Dystrophy
... > Musculoskeletal Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophy, Emery-Dreifuss > X-Linked Emery-Dreifuss Muscular Dystrophy
... > Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophy, Emery-Dreifuss > X-Linked Emery-Dreifuss Muscular Dystrophy

Preferred term

X-Linked Emery-Dreifuss Muscular Dystrophy  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Benign Scapuloperoneal Muscular Dystrophy with Early Contractures
  • Scapuloperoneal Syndrome, X Linked
  • Scapuloperoneal Syndrome, X-Linked
  • X-Linked Scapuloperoneal Syndrome

Scope note

  • 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.

History note

  • 2021

In other languages

URI

http://www.yso.fi/onto/mesh/D000083143

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